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2. Kellogg Eye Center

Definition, symptoms, and treatment of Retinoschisis.

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Retina > Retinoschisis

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Retinoschisis defined, description of symptoms, and information on treatment...
Retinoschisis is a disease of the nerve tissue in the eye. It affects the retinal cells in the macula (the central fixation point of vision at the back of the eye). Retinoschisis is technically a form of macular degeneration. However there are different types of and many people diagnosed with

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3. Retinoschisis Sequence Variation Database

Listing of all allelic variants in the RS1 gene.

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Retina > Retinoschisis

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Human and Clinical Genetics - Leiden University Medical Center X-linked Retinoschisis sequence variation database (modified last January 24, 2008) The Retinoschisis Web-site and sequence variation database was initiated through the maintained by Dr J.T. den Dunnen. If you have any interesting
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4. Retinoschisis - Wikipedia

Summarizes the known facts about the disease.

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Retina > Retinoschisis

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From Wikipedia, the free encyclopedia Classification and external resources disease characterized by the abnormal splitting of the 's neurosensory layers, usually in the , resulting in a loss of vision in the corresponding visual field in some rarer forms. More common forms are usually
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5. Handbook of Ocular Disease Management - Acquired Retinoschisis

Detailing signs and symptoms and pathophysiology.

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Retina > Retinoschisis

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The page you are looking for might have been removed, had its name changed, or is temporarily unavailable. Please try the following: Make sure that the Web site address displayed in the address bar of your browser is spelled and formatted correctly. If you reached this page by clicking a link,
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6. RS links

Jon Diercks's links about X-Linked Recessive Juvenile Retinoschisis.

Category:

Retina > Retinoschisis

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X-Linked Recessive Juvenile Retinoschisis (RS) Retinoschisis causes the layers of the retina to separate from each other, distorting the visual image in such a way that it cannot be at the National Organization for Rare Disorders (NORD) RS is passed from parent to child via a recessive gene on
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