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Archive for the ‘Eye Sight & Vision’ Category

Human eye – Wikipedia, the free encyclopedia

Friday, June 5th, 2015

The human eye is an organ that reacts to light and has several purposes. As a sense organ, the mammalian eye allows vision. Rod and cone cells in the retina allow conscious light perception and vision including color differentiation and the perception of depth. The human eye can distinguish about 10 million colors.[1]

Similar to the eyes of other mammals, the human eye's non-image-forming photosensitive ganglion cells in the retina receive light signals which affect adjustment of the size of the pupil, regulation and suppression of the hormone melatonin and entrainment of the body clock.[2]

The eye is not shaped like a perfect sphere, rather it is a fused two-piece unit. The smaller frontal unit, more curved, called the cornea is linked to the larger unit called the sclera. The corneal segment is typically about 8mm (0.3in) in radius. The sclerotic chamber constitutes the remaining five-sixths; its radius is typically about 12mm. The cornea and sclera are connected by a ring called the limbus. The iris the color of the eye and its black center, the pupil, are seen instead of the cornea due to the cornea's transparency. To see inside the eye, an ophthalmoscope is needed, since light is not reflected out.

The dimensions differ among adults by only one or two millimeters; it is remarkably consistent across different ethnicities. The vertical measure, generally less than the horizontal distance, is about 24mm among adults, at birth about 1617 millimeters (about 0.65inch). The eyeball grows rapidly, increasing to 22.523mm (approx. 0.89 in) by three years of age. By age 13, the eye attains its full size. The typical adult eye has an anterior to posterior diameter of 24 millimeters, a volume of six cubic centimeters (0.4 cu. in.),[3] and a mass of 7.5 grams (weight of 0.25 oz.).[citation needed]

The eye is made up of three coats, enclosing three transparent structures. The outermost layer, known as the fibrous tunic, is composed of the cornea and sclera. The middle layer, known as the vascular tunic or uvea, consists of the choroid, ciliary body, and iris. The innermost is the retina, which gets its circulation from the vessels of the choroid as well as the retinal vessels, which can be seen in an ophthalmoscope.

Within these coats are the aqueous humour, the vitreous body, and the flexible lens. The aqueous humour is a clear fluid that is contained in two areas: the anterior chamber between the cornea and the iris, and the posterior chamber between the iris and the lens. The lens is suspended to the ciliary body by the suspensory ligament (Zonule of Zinn), made up of fine transparent fibers. The vitreous body is a clear jelly that is much larger than the aqueous humour present behind the lens, and the rest is bordered by the sclera, zonule, and lens. They are connected via the pupil.[4]

The approximate field of view of an individual human eye is 95 away from the nose, 75 downward, 60 toward the nose, and 60 upward, allowing humans to have an almost 180-degree forward-facing horizontal field of view.[citation needed] With eyeball rotation of about 90 (head rotation excluded, peripheral vision included), horizontal field of view is as high as 270. About 1215 temporal and 1.5 below the horizontal is the optic nerve or blind spot which is roughly 7.5 high and 5.5 wide.[5]

The retina has a static contrast ratio of around 100:1 (about 6.5 f-stops). As soon as the eye moves (saccades) it re-adjusts its exposure both chemically and geometrically by adjusting the iris which regulates the size of the pupil. Initial dark adaptation takes place in approximately four seconds of profound, uninterrupted darkness; full adaptation through adjustments in retinal chemistry (the Purkinje effect) is mostly complete in thirty minutes. The process is nonlinear and multifaceted, so an interruption by light merely starts the adaptation process over again. Full adaptation is dependent on good blood flow; thus dark adaptation may be hampered by poor circulation, and vasoconstrictors like tobacco.[citation needed]

The human eye can detect a luminance range of 1014, or one hundred trillion (100,000,000,000,000) (about 46.5 f-stops), from 106 cd/m2, or one millionth (0.000001) of a candela per square meter to 108 cd/m2 or one hundred million (100,000,000) candelas per square meter.[6][7][8] This range does not include looking at the midday sun (109 cd/m2)[9] or lightning discharge.

At the low end of the range is the absolute threshold of vision for a steady light across a wide field of view, about 106 cd/m2 (0.000001 candela per square meter).[10][11] The upper end of the range is given in terms of normal visual performance as 108 cd/m2 (100,000,000 or one hundred million candelas per square meter).[12]

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Visual perception – Wikipedia, the free encyclopedia

Monday, June 1st, 2015

Visual perception is the ability to interpret the surrounding environment by processing information that is contained in visible light. The resulting perception is also known as eyesight, sight, or vision (adjectival form: visual, optical, or ocular). The various physiological components involved in vision are referred to collectively as the visual system, and are the focus of much research in psychology, cognitive science, neuroscience, and molecular biology, collectively referred to as vision science.

The visual system in animals allows individuals to assimilate information from their surroundings. The act of seeing starts when the lens of the eye focuses an image of its surroundings onto a light-sensitive membrane in the back of the eye, called the retina. The retina is actually part of the brain that is isolated to serve as a transducer for the conversion of patterns of light into neuronal signals. The lens of the eye focuses light on the photoreceptive cells of the retina, which detect the photons of light and respond by producing neural impulses. These signals are processed in a hierarchical fashion by different parts of the brain, from the retina upstream to central ganglia in the brain.

Note that up until now much of the above paragraph could apply to octopi, mollusks, worms, insects and things more primitive; anything with a more concentrated nervous system and better eyes than say a jellyfish. However, the following applies to mammals generally and birds (in modified form): The retina in these more complex animals sends fibers (the optic nerve) to the lateral geniculate nucleus, to the primary and secondary visual cortex of the brain. Signals from the retina can also travel directly from the retina to the superior colliculus.

The perception of objects and the totality of the visual scene is accomplished by the visual association cortex. The visual association cortex combines all sensory information perceived by the striate cortex which contains thousands of modules that are part of modular neural networks. The neurons in the striate cortex send axons to the extrastriate cortex, a region in the visual association cortex that surrounds the striate cortex.[1]

The major problem in visual perception is that what people see is not simply a translation of retinal stimuli (i.e., the image on the retina). Thus people interested in perception have long struggled to explain what visual processing does to create what is actually seen.

There were two major ancient Greek schools, providing a primitive explanation of how vision is carried out in the body.

The first was the "emission theory" which maintained that vision occurs when rays emanate from the eyes and are intercepted by visual objects. If an object was seen directly it was by 'means of rays' coming out of the eyes and again falling on the object. A refracted image was, however, seen by 'means of rays' as well, which came out of the eyes, traversed through the air, and after refraction, fell on the visible object which was sighted as the result of the movement of the rays from the eye. This theory was championed by scholars like Euclid and Ptolemy and their followers.

The second school advocated the so-called 'intro-mission' approach which sees vision as coming from something entering the eyes representative of the object. With its main propagators Aristotle, Galen and their followers, this theory seems to have some contact with modern theories of what vision really is, but it remained only a speculation lacking any experimental foundation.

Both schools of thought relied upon the principle that "like is only known by like", and thus upon the notion that the eye was composed of some "internal fire" which interacted with the "external fire" of visible light and made vision possible. Plato makes this assertion in his dialogue Timaeus, as does Aristotle, in his De Sensu.[2]

Alhazen (965c. 1040) carried out many investigations and experiments on visual perception, extended the work of Ptolemy on binocular vision, and commented on the anatomical works of Galen.[3][4]

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Autism Spectrum Disorders, Vision, and Eyesight – Autistic …

Sunday, May 24th, 2015

If you are looking for an eye doctor for a person with autism or suspected autism spectrum disorders, locate a behavioral or neuro-developmental optometrist and ask the following questions before scheduling the eye examination: (1) Does the optometrist (1) have experience in evaluating the vision of a non-verbal and/or autistic person? and (2) If appropriate to the individual case, does the optometrist offer special corrective lenses for autistic individuals (i.e., prisms, microprisms, colored lenses and/or filters)? Prior to using the special ambient lenses, Zarin had a problem with spatial awareness. He would bang through doorways and slam through people...he doesn't do that anymore ... his gait has changed ... his ability to express himself, it is much better now ... [More]

We thought his eye movements and eye symptoms were just part of his autism, but...with vision therapy treatment, many of his so-called "autistic" behaviors stopped, and he was also able to read much easier (no more double vision!)... [More]

I am the parent of an autistic child. Too often, visual problems which would have been detected early in non-disabled children go undiagnosed and untreated for children with disabilities ... Don't assume that your child can't be tested ... [More]

He had only had his special prescription eyeglasses for thirty minutes and already our lives were changed ... Jimmy began to visually investigate his immediate environment ... he makes eye contact while communicating ... was basically non-verbal a year ago, and now uses speech to communicate ...all of his other therapies have benefited from vision therapy as well his progress in speech therapy which has sky rocketed! [More]

Since beginning Vision Therapy, she has been able to remain in control (with reminders to stay focused) and sit on her own with others for as long as 30 minutes, this is something she could not do 7 months ago. [More]

... Evelyn is now a year ahead of her chronological age in vision skills! [More]

Donna Williams, a well-known author with autism ... stated that when she put on her glasses for the first time, "the room didn't seem so crowded, overwhelming or bombarding. The background noise I had always heard before was not even apparent." [More]

The poor eye contact, toe walking, and odd neck and body postures of many autistic individuals may be due to vision problems, according to a study that suggests that these abnormal symptoms can be reduced by corrective lenses. [More]

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I am the parent of an autistic child.

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All About Eyes | "Your Sight is My Vision"

Thursday, May 21st, 2015

Technology: Patient Care Apps; Increased Practice Efficiency.

Apps are everywhere, and have the potential to play an important role in patient care. Downloading apps will soon be an American tradition, similar to back in the day when fathers chased their kids around with power tools. I told my boss I was turning thirty and getting my first smartphone, he smiled and said he had socks older than me. So, I did what any new associate would do. I bought him new socks. He chased me around the office with an alger brush.

Turns out your smartphone and sock drawer have more in common than you think. When I was a youngster, not a whole lot went into the sock drawer. It wasnt hard to reach in and grab a matching pair. The older I get though, the more socks go into the drawer and its much harder to find two that go together. In fact, I have a lot of lonesome socks. Studies have shown, if the missing sock does not reappear within the first 24 hours, your chances of finding that sock decrease by 75%. Sounds like my practice consultant on uncollected Co-pays. The same applies to my phone, the longer I have it the more junk it collects. I have a bunch of old apps cluttering my wallpaper in hopes one day Ill actually use that Ab workout app I downloaded months ago.

Therefore, if you havent updated your smart phone or tablet devices this year, youre likely in the floppy disk age of apps. So if youre like me its time to ditch those lonely socks, stop living life in the cheap seats and get yourself some sexier apps!

1. Parks 3-step (Cost: $0.99)

Have a patient with double vision?? Theres an app for that, seriously. There can be many reasons patients have diplopia. Its possible they need prism, vision therapy, or need to lay off the eyeball martinis. Or they may have a paretic extraocular muscle and you need to diagnose it. If youve forgotten everything about the parks 3 step except it involves hypers, obliques and head tilts you need the Parks 3-step app. It utilizes your devices built-in gyroscope and accelerometer to predict the paretic EOM in two swift movements. Enjoy!

Pros: Simple, quick, accurate way of performing the Parks 3-step without diagrams.

Cons: Needs option to input data manually in addition to turning phone and some updated animations.

2. Medical Lab Tests (Cost: $2.99)

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Blurry Eye Vision Blurred Vision, and Cures for Blurry …

Tuesday, May 19th, 2015

by admin on February 14, 2012

Are you a patient suffering from blurred vision in the left eye? There are two types of blurred vision instances that the patient can be suffering from. The first instance includes the patient suffering from gradual blurred vision in the left eye and the second instance indicates a patient that is suffering from sudden blurred vision in the left eye.

Though there are many causes for each of these types of cases, it is important for the patient suffering from sudden blurred vision in the left eye to schedule an appointment with an optometrist or schedule an appointment with their family doctor to try and narrow down the cause of the blurred vision in the left eye.

Have you had any sudden trauma to the left eye? Many times, trauma to the left eye can create blurred vision in that eye for a period of between two to four days as the eye heals from the injury. However, if you have suffered from a trauma to the left eye and are suffering from blurred vision, you just might want to check with the local health care professional to ensure that there has been no damage to the eye.

Blurred vision has a number of causes, aside from trauma, but the causes become more worrisome when it is one eye that is suffering from the blurred vision, in contrast to both of the eyes suffering from blurred vision.

It is important to consider all of the options and consider all of the causes of blurred vision to ensure that the patient is going to have adequate medical attention and avoid any repercussions from the cause of the blurred vision.

A simple appointment with a doctor or optometrist can help to rule out any damage done to the eye and is recommended for those suffering from blurred vision.

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6 Tips for Eye Health and Maintaining Good Eyesight

Tuesday, May 19th, 2015

Don't take your eyes for granted. Protect your sight with these six tips:

Protecting your eyes starts with the food on your plate. Nutrients such as omega-3 fatty acids, lutein, zinc, and vitamins C and E might help ward off age-related vision problems such as macular degeneration and cataracts, studies show. Regularly eating these foods can help lead to good eye health:

Eating a well-balanced diet also helps you maintain a healthy weight, which makes you less likely to get obesity-related diseases such as type 2 diabetes. Diabetes is the leading cause of blindness in adults.

Smoking makes you more likely to get cataracts, optic nerve damage, and macular degeneration. If you've tried to quit smoking before and started smoking again, keep trying. The more times you try to quit smoking, the more likely you are to succeed.

The right kind of sunglasses will help protect your eyes from the sun's ultraviolet (UV) rays.

Too much UV exposure makes you more likely to get cataracts and macular degeneration.

Choose sunglasses that block 99% to 100% of both UVA and UVB rays. Wraparound lenses help protect your eyes from the side. Polarized lenses reduce glare when driving.

If you wear contact lenses, some offer UV protection. It's still a good idea to wear sunglasses for more protection, though.

If you work with hazardous or airborne materials on the job or at home, wear safety glasses or protective goggles every time.

Certain sports such as ice hockey, racquetball, and lacrosse can also lead to eye injury. Wear eye protection (such as helmets with protective face masks or sports goggles with polycarbonate lenses) to shield your eyes.

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Mum tells of delight at pioneering eye operation which has helped restore her sight

Wednesday, May 23rd, 2012

May 22 2012 By Jack Mathieson

sylvia paton Image 3

A BRAVE Scots mum agreed to be a guinea pig for a pioneering stem cell eye operation which could help millions of people see.

Sylvia Paton, 50, who has just a tenth of normal vision, had stem cells transplanted into her eye in the first op of its kind in the UK.

And she hopes the pioneering technique being developed by Scots scientists will help other sufferers of her condition, known as corneal blindness.

She said yesterday: If we dont have guinea pigs we cant learn anything, and Im quite happy for them to learn from me.

Im so excited about the possibilities of this procedure. It has the potential to save vision, protect and give back vision to people like me.

Even if only a little of my vision is restored, it would be better than nothing.

Sylvia, of Corstorphine, Edinburgh, a PA for the Scottish Government, was born without an iris in her left eye. As a result, the cornea in the eye became damaged, badly affecting her vision.

She also has a cataract in the eye and her sight is getting worse as she ages. Her son Michael, 23, has the same condition, which made her even more determined to have the op.

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Glaucoma: A Neurological Disorder?

Wednesday, March 14th, 2012

By Traci Pedersen Associate News Editor Reviewed by John M. Grohol, Psy.D. on March 11, 2012

A novel explanation of glaucoma is rapidly rising, and it is promoting advances in treatment that may ultimately eliminate the disease. Rather than being viewed solely as an eye disease, top scientists now consider glaucoma to be a neurologic disorder that causes nerve cell death, similar to what happens in Parkinsons disease and Alzheimers.

Treatment advances are being tested in patients or are scheduled to begin clinical trials soon.

The long-standing theory regarding glaucoma was that vision damage was caused by unusually high pressure inside the eye, known as intraocular pressure (IOP). Therefore, lowering IOP was the focus of surgical techniques and medications; developing tests and instruments to measure and track IOP was vital to that effort.

Although measuring a patients IOP is still a key part of glaucoma treatment, it is no longer the only method an ophthalmologist uses to diagnose glaucoma. Even when surgery or medication successfully lowers IOP, some glaucoma patients continue to lose vision.

Also, some patients find it difficult to use eye drop medications as prescribed by their physicians. These problems encouraged researchers to look beyond IOP as a cause of glaucoma and focus of treatment.

The new research model focuses on the damage that occurs in a type of nerve cell called retinal ganglion cells (RGCs), which connect the eye to the brain through the optic nerve and are vital to vision.

RGC-targeted glaucoma treatments now in clinical trials include: medications injected into the eye that deliver survival and growth factors to RGCs; medications known to be useful for stroke and Alzheimers, such as cytidine-5-diphosphocholine; and electrical stimulation of RGCs, delivered through tiny electrodes implanted in contact lenses or other external devices. Human trials of stem cell therapies are in the planning stages.

As researchers turn their attention to the mechanisms that cause retinal ganglion cells to degenerate and die, they are discovering ways to protect, enhance and even regenerate these vital cells, said Jeffrey L Goldberg, M.D., Ph.D., assistant professor of ophthalmology at the Bascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute.

Understanding how to prevent damage and improve healthy function in these neurons may ultimately lead to sight-saving treatments for glaucoma and other degenerative eye diseases.

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Human stem cells 'help blind rat'

Thursday, March 8th, 2012

7 March 2012 Last updated at 11:47 ET By James Gallagher Health and science reporter, BBC News

Stem cells taken from the back of a human eye have restored some vision to blind rats, according to researchers.

They say the findings could help treat blindness, caused by glaucoma, if similar results can be repeated in humans.

The study, published in the journal Stem Cells Translational Medicine, used the cells to form new nerves in the eye.

These hooked up with the existing nerves, restoring sight.

Glaucoma can lead to blindness and is caused by a build-up of pressure within the eye. This kills retinal ganglion cells, the nerves which take information from the retina and pass it onto the brain.

Researchers at University College London and Moorfields Eye Hospital believe they have regenerated the retinal ganglion cells using human stem cells.

With permission from families, cell samples were taken from eyes which had been donated for cornea transplants.

It is a significant step towards our ultimate goal of finding a cure for glaucoma and other related conditions

Very rare cells in the eye, Muller glia stem cells, were collected. These were grown in the laboratory and converted into retinal ganglion cells.

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New research characterizes glaucoma as neurologic disorder rather than eye disease

Thursday, March 8th, 2012

Public release date: 6-Mar-2012 [ | E-mail | Share ]

Contact: Mary Wade mwade@aao.org 415-447-0221 American Academy of Ophthalmology

SAN FRANCISCO March 6, 2012 A new paradigm to explain glaucoma is rapidly emerging, and it is generating brain-based treatment advances that may ultimately vanquish the disease known as the "sneak thief of sight." A review now available in Ophthalmology, the journal of the American Academy of Ophthalmology, reports that some top researchers no longer think of glaucoma solely as an eye disease. Instead, they view it as a neurologic disorder that causes nerve cells in the brain to degenerate and die, similar to what occurs in Parkinson disease and in Alzheimer's. The review, led by Jeffrey L Goldberg, M.D., Ph.D., assistant professor of ophthalmology at the Bascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute, describes treatment advances that are either being tested in patients or are scheduled to begin clinical trials soon.

Glaucoma is the most common cause of irreversible blindness worldwide. For many years, the prevailing theory was that vision damage in glaucoma patients was caused by abnormally high pressure inside the eye, known as intraocular pressure (IOP). As a result, lowering IOP was the only goal of those who developed surgical techniques and medications to treat glaucoma. Creating tests and instruments to measure and track IOP was crucial to that effort. Today, a patient's IOP is no longer the only measurement an ophthalmologist uses to diagnose glaucoma, although it is still a key part of deciding how to care for the patient. IOP-lowering medications and surgical techniques continue to be effective ways to protect glaucoma patients' eyes and vision. Tracking changes in IOP over time informs the doctor whether the treatment plan is working.

But even when surgery or medication successfully lowers IOP, vision loss continues in some glaucoma patients. Also, some patients find it difficult to use eye drop medications as prescribed by their physicians. These significant shortcomings spurred researchers to look beyond IOP as a cause of glaucoma and focus of treatment.

The new research paradigm focuses on the damage that occurs in a type of nerve cell called retinal ganglion cells (RGCs), which are vital to the ability to see. These cells connect the eye to the brain through the optic nerve.

RGC-targeted glaucoma treatments now in clinical trials include: medications injected into the eye that deliver survival and growth factors to RGCs; medications known to be useful for stroke and Alzheimer's, such as cytidine-5-diphosphocholine; and electrical stimulation of RGCs, delivered via tiny electrodes implanted in contact lenses or other external devices. Human trials of stem cell therapies are in the planning stages.

"As researchers turn their attention to the mechanisms that cause retinal ganglion cells to degenerate and die, they are discovering ways to protect, enhance and even regenerate these vital cells," said Dr. Goldberg. "Understanding how to prevent damage and improve healthy function in these neurons may ultimately lead to sight-saving treatments for glaucoma and other degenerative eye diseases."

If this neurologically-based research succeeds, future glaucoma treatments may not only prevent glaucoma from stealing patients' eyesight, but may actually restore vision. Scientists also hope that their in-depth exploration of RGCs will help them determine what factors, such as genetics, make some people more vulnerable to glaucoma.

###

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New Research Characterizes Glaucoma as a Neurologic Disorder Rather Than an Eye Disease

Wednesday, March 7th, 2012

SAN FRANCISCO, CA--(Marketwire -03/06/12)- A new paradigm to explain glaucoma is rapidly emerging, and it is generating brain-based treatment advances that may ultimately vanquish the disease known as the "sneak thief of sight." A review now available in Ophthalmology, the journal of the American Academy of Ophthalmology, reports that some top researchers no longer think of glaucoma solely as an eye disease. Instead, they view it as a neurologic disorder that causes nerve cells in the brain to degenerate and die, similar to what occurs in Alzheimer's and in Parkinson's disease. The review, led by Jeffrey L Goldberg, M.D., Ph.D., assistant professor of ophthalmology at the Bascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute, describes treatment advances that are either being tested in patients or are scheduled to begin clinical trials soon.

Glaucoma is the most common cause of irreversible blindness worldwide. For many years, the prevailing theory was that vision damage in glaucoma patients was caused by abnormally high pressure inside the eye, known as intraocular pressure (IOP). As a result, lowering IOP was the only goal of those who developed surgical techniques and medications to treat glaucoma. Creating tests and instruments to measure and track IOP was crucial to that effort. Today, a patient's IOP is no longer the only measurement an ophthalmologist uses to diagnose glaucoma, although it is still a key part of deciding how to care for the patient. IOP-lowering medications and surgical techniques continue to be effective ways to protect glaucoma patients' eyes and vision. Tracking changes in IOP over time informs the doctor whether the treatment plan is working.

But even when surgery or medication successfully lowers IOP, vision loss continues in some glaucoma patients. Also, some patients find it difficult to use eye drop medications as prescribed by their physicians. These significant shortcomings spurred researchers to look beyond IOP as a cause of glaucoma and focus of treatment.

The new research paradigm focuses on the damage that occurs in a type of nerve cell called retinal ganglion cells (RGCs), which are vital to the ability to see. These cells connect the eye to the brain through the optic nerve.

RGC-targeted glaucoma treatments now in clinical trials include: medications injected into the eye that deliver survival and growth factors to RGCs; medications known to be useful for stroke and Alzheimer's, such as cytidine-5-diphosphocholine; and electrical stimulation of RGCs, delivered via tiny electrodes implanted in contact lenses or other external devices. Human trials of stem cell therapies are in the planning stages.

"As researchers turn their attention to the mechanisms that cause retinal ganglion cells to degenerate and die, they are discovering ways to protect, enhance and even regenerate these vital cells," said Dr. Goldberg. "Understanding how to prevent damage and improve healthy function in these neurons may ultimately lead to sight-saving treatments for glaucoma and other degenerative eye diseases."

If this neurologically-based research succeeds, future glaucoma treatments may not only prevent glaucoma from stealing patients' eyesight, but may actually restore vision. Scientists also hope that their in-depth exploration of RGCs will help them determine what factors, such as genetics, make some people more vulnerable to glaucoma.

Note to media: Contact Media Relations to request full text of the study, arrange interviews with experts, and request images.

About the American Academy of OphthalmologyThe American Academy of Ophthalmology is the world's largest association of eye physicians and surgeons -- Eye M.D.s -- with more than 30,000 members worldwide. Eye health care is provided by the three "O's" -- ophthalmologists, optometrists, and opticians. It is the ophthalmologist, or Eye M.D., who can treat it all: eye diseases, infections and injuries, and perform eye surgery. For more information, visit http://www.aao.org. The Academy's EyeSmart public education program works to educate the public about the importance of eye health and to empower them to preserve their healthy vision, by providing the most trusted and medically accurate information about eye diseases, conditions and injuries. Visit http://www.geteyesmart.org to learn more.

About OphthalmologyOphthalmology, the official journal of the American Academy of Ophthalmology, publishes original, peer-reviewed reports of research in ophthalmology, including basic science investigations and clinical studies. Topics include new diagnostic and surgical techniques, treatment methods, instrument updates, the latest drug findings, results of clinical trials, and research findings. Ophthalmology also publishes major reviews of specific topics by acknowledged authorities.

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Advanced Cell Technology Announces Approval of Wills Eye Institute as Additional Site for Stem Cell Clinical Trial for …

Thursday, February 16th, 2012

MARLBOROUGH, Mass.--(BUSINESS WIRE)--

Advanced Cell Technology, Inc. (“ACT”; OTCBB: ACTC), a leader in the field of regenerative medicine, announced today that the Wills Eye Institute in Philadelphia has received institutional review board (IRB) approval as a site for the company’s Phase I/II clinical trial for Stargardt’s Macular Dystrophy (SMD), a form of juvenile macular degeneration, using human embryonic stem cell (hESC)-derived retinal pigment epithelial (RPE) cells. Earlier this year, the Company also announced that the IRB at Wills Eye Institute had approved the participation of the institution as a site for ACT’s clinical trial for dry age-related macular degeneration (dry AMD).

“We thank Wills Eye Institute once more for providing their IRB and their invaluable contribution to our macular degeneration studies,” said Gary Rabin, ACT’s chairman and CEO. “We are very happy that we can now report that Wills Eye Institute has been approved as a clinical trial site for both our SMD and dry AMD clinical trials. Ranked as one of the best ophthalmology hospitals in the country by U.S. News & World Report, the Wills Eye Institute is a truly world-class institution. Our team is eagerly anticipating working with Dr. Carl Regillo, a renowned retinal surgeon and director of clinical retina research at Wills Eye Institute, as well as a professor of ophthalmology at Thomas Jefferson University, along with the rest of his team as we move forward with these ground-breaking trials.”

The Phase I/II trial for SMD is a prospective, open-label study designed to determine the safety and tolerability of the hESC-derived RPE cells following sub-retinal transplantation into patients with SMD. The trial will ultimately enroll 12 patients, with cohorts of three patients each in an ascending dosage format. Preliminary results relating to both early safety and biological function for the first two patients in the U.S., one SMD patient and one dry AMD patient, were recently reported in The Lancet.

Specific patient enrollment for both trials at the Wills Eye Institute will be determined in the near future. Further information about patient eligibility for the SMD study and the concurrent study on dry AMD is also available on http://www.clinicaltrials.gov; ClinicalTrials.gov Identifiers: NCT01345006 and NCT01344993.

About Stargardt's Disease

Stargardt’s disease or Stargardt’s Macular Dystrophy is a genetic disease that causes progressive vision loss, usually starting in children between 10 to 20 years of age. Eventually, blindness results from photoreceptor loss associated with degeneration in the pigmented layer of the retina, called the retinal pigment epithelium.

About hESC-derived RPE Cells

The retinal pigment epithelium (RPE) is a highly specialized tissue located between the choroids and the neural retina. RPE cells support, protect and provide nutrition for the light-sensitive photoreceptors. Human embryonic stem cells differentiate into any cell type, including RPE cells, and have a similar expression of RPE-specific genes compared to human RPE cells and demonstrate the full transition from the hESC state.

About Advanced Cell Technology, Inc.

Advanced Cell Technology, Inc., is a biotechnology company applying cellular technology in the field of regenerative medicine. For more information, visit http://www.advancedcell.com.

About Wills Eye Institute

Wills Eye Institute is a global leader in ophthalmology, established in 1832 as the nation’s first hospital specializing in eye care. U.S. News & World Report has consistently ranked Wills Eye as one of America’s top three ophthalmology centers since the survey began in 1990. Wills Eye is a premier training site for all levels of medical education. Its resident and post-graduate training programs are among the most competitive in the country. One of the core strengths of Wills is the close connection between innovative research and advanced patient care. Wills provides the full range of primary and subspecialty eye care for improving and preserving sight, including cataract, cornea, retina, emergency care, glaucoma, neuro-ophthalmology, ocular oncology, oculoplastics, pathology, pediatric ophthalmology and ocular genetics, refractive surgery and retina. Ocular Services include the Wills Laser Correction Center, Low Vision Service, and Diagnostic Center. Its 24/7 Emergency Service is the only one of its kind in the region. Wills Eye also has a network of nine multi-specialty, ambulatory surgery centers throughout the tri-state area. To learn more, please visit http://www.willseye.org.

Forward-Looking Statements

Statements in this news release regarding future financial and operating results, future growth in research and development programs, potential applications of our technology, opportunities for the company and any other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Any statements that are not statements of historical fact (including statements containing the words “will,” “believes,” “plans,” “anticipates,” “expects,” “estimates,” and similar expressions) should also be considered to be forward-looking statements. There are a number of important factors that could cause actual results or events to differ materially from those indicated by such forward-looking statements, including: limited operating history, need for future capital, risks inherent in the development and commercialization of potential products, protection of our intellectual property, and economic conditions generally. Additional information on potential factors that could affect our results and other risks and uncertainties are detailed from time to time in the company’s periodic reports, including the report on Form 10-K for the year ended December 31, 2010. Forward-looking statements are based on the beliefs, opinions, and expectations of the company’s management at the time they are made, and the company does not assume any obligation to update its forward-looking statements if those beliefs, opinions, expectations, or other circumstances should change. Forward-looking statements are based on the beliefs, opinions, and expectations of the company’s management at the time they are made, and the company does not assume any obligation to update its forward-looking statements if those beliefs, opinions, expectations, or other circumstances should change. There can be no assurance that the Company’s clinical trials will be successful.

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Advanced Cell Technology Announces Approval of Wills Eye Institute as Additional Site for Stem Cell Clinical Trial for ...

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Burn Victim Eye Sight Restored with Stem Cell Therapy

Tuesday, June 29th, 2010

Doctors are saying stem cell transplants are a promising new treatment to restore sight to individuals who have suffered severe eye damage. Dozens of patients whose eyes were injured after being splashed with caustic chemicals were able to see again after receiving a transplant of their own stem cells, according to The Associated Press.

Italian researchers reported that the transplants had worked completely in 82 of 107 eyes, including in one patient who sustained severe eye injuries some 60 years ago and has had his sight almost completely restored. The transplant worked at least partially in 14 other eyes, and the benefits have lasted for up to 10 years.

"This is great work, an absolutely great way to do it," said Dr. Douglas Lazzaro, chairman of ophthalmology at Long Island College Hospital. "It can only increase the success rate of these types of procedures."

Dr. Bruce Rosenthal, chief of low-vision programs at Lighthouse International, a nonprofit that fights vision impairment, called the stem cell transplants a very promising treatment. The procedure bypasses the risk of rejection posed by corneal transplants because the patient’s own stem cells are used.

"This is a major step in returning vision to someone who has lost it," Rosenthal says.

University of California ophthalmologist Ivan Schwab, who is not involved in the study, called the research "a roaring success."

Each year, stem cell transplants could offer the promise of healing to thousands of people who sustain chemical burns on their corneas, although they would not help those with macular degeneration, which involves the eye’s retina, or those with damage to the optic nerve. People who are blind in both eyes also would not be candidates for the transplant because some healthy tissue is required to undergo it, doctors explained.

The researchers who performed the transplants for the study, which was published online by the New England Journal of Medicine, removed stem cells from the patient’s good eye, grew them in the lab and put them back in the injured eye. There, they grew new corneal tissue that replaced the damaged tissue. None of the patients needed anti-rejection drugs.

For many years, adult stem cells have been used to treat disorders as varied as leukemia and sickle cell anemia. But fixing damaged eyes with a stem cell transplant is relatively new - and so far is not being done here.

"The U.S. is pretty stringent," Rosenthal says. "They won’t allow these procedures until they are FDA-approved and have gone through a lot of clinical testing. But even though it’s not ready for prime time, there is a lot of hope for the future."

Some 61 million Americans are at high risk for serious vision loss, according to Lighthouse International, and about 61 million individuals age 45 and older will have vision loss by 2015. A Lighthouse survey revealed that fewer than half (46%) of Americans get an annual eye exam.

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Stem Cells improve or reverse problems associated with Blindness, Eye Sight and Vision

Friday, June 25th, 2010

Stem cells reverse blindness caused by burns

By ALICIA CHANG (AP) – 1 day ago

LOS ANGELES — Dozens of people who were blinded or otherwise suffered severe eye damage when they were splashed with caustic chemicals had their sight restored with transplants of their own stem cells — a stunning success for the burgeoning cell-therapy field, Italian researchers reported Wednesday.

The treatment worked completely in 82 of 107 eyes and partially in 14 others, with benefits lasting up to a decade so far. One man whose eyes were severely damaged more than 60 years ago now has near-normal vision.

"This is a roaring success," said ophthalmologist Dr. Ivan Schwab of the University of California, Davis, who had no role in the study — the longest and largest of its kind.

Stem cell transplants offer hope to the thousands of people worldwide every year who suffer chemical burns on their corneas from heavy-duty cleansers or other substances at work or at home.

The approach would not help people with damage to the optic nerve or macular degeneration, which involves the retina. Nor would it work in people who are completely blind in both eyes, because doctors need at least some healthy tissue that they can transplant.

In the study, published online by the New England Journal of Medicine, researchers took a small number of stem cells from a patient's healthy eye, multiplied them in the lab and placed them into the burned eye, where they were able to grow new corneal tissue to replace what had been damaged. Since the stem cells are from their own bodies, the patients do not need to take anti-rejection drugs.

Adult stem cells have been used for decades to cure blood cancers such as leukemia and diseases like sickle cell anemia. But fixing a problem like damaged eyes is a relatively new use. Researchers have been studying cell therapy for a host of other diseases, including diabetes and heart failure, with limited success.

Adult stem cells, which are found around the body, are different from embryonic stem cells, which come from human embryos and have stirred ethical concerns because removing the cells requires destroying the embryos.

Currently, people with eye burns can get an artificial cornea, a procedure that carries such complications as infection and glaucoma, or they can receive a transplant using stem cells from a cadaver, but that requires taking drugs to prevent rejection.

The Italian study involved 106 patients treated between 1998 and 2007. Most had extensive damage in one eye, and some had such limited vision that they could only sense light, count fingers or perceive hand motions. Many had been blind for years and had had unsuccessful operations to restore their vision.

The cells were taken from the limbus, the rim around the cornea, the clear window that covers the colored part of the eye. In a normal eye, stem cells in the limbus are like factories, churning out new cells to replace dead corneal cells. When an injury kills off the stem cells, scar tissue forms over the cornea, clouding vision and causing blindness.

In the Italian study, the doctors removed scar tissue over the cornea and glued the laboratory-grown stem cells over the injured eye. In cases where both eyes were damaged by burns, cells were taken from an unaffected part of the limbus.

Researchers followed the patients for an average of three years and some as long as a decade. More than three-quarters regained sight after the transplant. An additional 13 percent were considered a partial success. Though their vision improved, they still had some cloudiness in the cornea.

Patients with superficial damage were able to see within one to two months. Those with more extensive injuries took several months longer.

"They were incredibly happy. Some said it was a miracle," said one of the study leaders, Graziella Pellegrini of the University of Modena's Center for Regenerative Medicine in Italy. "It was not a miracle. It was simply a technique."

The study was partly funded by the Italian government.

Researchers in the United States have been testing a different way to use self-supplied stem cells, but that work is preliminary.

One of the successful transplants in the Italian study involved a man who had severe damage in both eyes as a result of a chemical burn in 1948. Doctors grafted stem cells from a small section of his left eye to both eyes. His vision is now close to normal.

In 2008, there were 2,850 work-related chemical burns to the eyes in the United States, according to the Bureau of Labor Statistics.

Schwab of UC Davis said stem cell transplants would not help those blinded by burns in both eyes because doctors need stem cells to do the procedure.

"I don't want to give the false hope that this will answer their prayers," he said.

Dr. Sophie Deng, a cornea expert at the UCLA's Jules Stein Eye Institute, said the biggest advantage was that the Italian doctors were able to expand the number of stem cells in the lab. This technique is less invasive than taking a large tissue sample from the eye and lowers the chance of an eye injury.

"The key is whether you can find a good stem cell population and expand it," she said.

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Online:

New England Journal: http://www.nejm.org

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