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Clinical Trials

August 31, 2018

Retina Foundation Participates in International Effort to Treat Stargardt Disease

Stargardt disease is the most common form of inherited juvenile macular degeneration. Stargardt disease begins in late childhood and may …

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Clinical Trials

April 19, 2018

First Patient in Phase 1/2 Clinical Study of Gene Therapy is Treated for X-Linked RP

The first human patient has been administered an AAV-based gene therapy treatment for x-linked retinitis pigmentosa (XLRP). This is an exciting …

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News/ Press Release

December 29, 2017

The Edward C. Fogg, III and Lisbeth A. Fogg Charitable Trust grants Retina Foundation $133,000 for Genetic Eye Disease

The Edward C. Fogg, III and Lisbeth A. Fogg Charitable Trust renewed their support for our Texas 1000 Project to identify …

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Patient Story

October 27, 2017

Gene Therapy Trial at the Retina Foundation of the Southwest featured in The Dallas Morning News

Mason Two Crow, 22, first came to the Retina Foundation in 2003 with a diagnosis of X-linked retinoschisis, a rare …

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News/ Press Release

July 18, 2017

Gene Causing Blindness Found in Texas Hispanic Families

The Retina Foundation has been a large part of a genetic study about Retinitis Pigmentosa (RP) with The University of …

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Clinical Trials

June 29, 2017

Rose-Silverthorne Retinal Degenerations Lab to Conduct Natural History Study of Usher Syndrome

The Rose-Silverthorne Retinal Degenerations Laboratory at the Retina Foundation of the Southwest is beginning a natural history trial to study …

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News/ Press Release

February 21, 2017

National Eye Institute Awards $949,804 for a 5-Year Study of RP

Lea Bennett, Ph.D., Postdoctoral Fellow, Rose-Silverthorne Retinal Degenerations Laboratory, studies inherited eye diseases under the direction of Dr. David Birch …

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News/ Press Release

August 2, 2016

Voelcker Fund Gives $100,000 in Support of Texas 1000 Project

The Max and Minnie Tomerlin Voelcker Fund recently gave a $100,000 gift to the Retina Foundation of the Southwest for …

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Patient Story

July 8, 2016

Early Detection is Critical for Rare Eye Diseases

Achromatopsia is a rare inherited eye disease characterized by decreased vision (20/200), extreme light sensitivity, and the absence of color …

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