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

Inherited Eye Diseases June 29, 2017

The Rose-Silverthorne Retinal Degenerations Laboratory at the Retina Foundation of the Southwest is beginning a natural history trial to study disease progression of Usher Syndrome Type 2a, a recessive genetic condition affecting nearly 25,000 people in the United States. Usher Syndrome Type 2a is categorized by patients born with mild to moderate hearing loss and vision loss from retinitis pigmentosa. Patients with Usher Syndrome Type 2a have a mutation of the gene USH2A. This study is expected to help us better understand USH2A-related retinal degeneration, develop new treatment options, and evaluate their effectiveness.

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

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