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Natural History and Genetic Studies of Usher Syndrome

$139,327N01FY2009EYNIH

The Emmes Company, Llc, Rockville MD

Investigators

Abstract

Natural History and Genetic Studies of Usher Syndrome This study will explore clinical and genetic aspects of Usher syndrome, an inherited disease causing deafness or impaired hearing, visual problems, and, in some cases, unsteadiness or balance problems. Patients with type 1 Usher syndrome usually are deaf from birth and have speech and balance problems. Patients with type 2 disease generally are hearing impaired but have no balance problems. Patients with type 3 disease have progressive hearing loss and balance problems. All patients develop retinitis pigmentosa, an eye disease that causes poor night vision and eventually, blindness.

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Natural History and Genetic Studies of Usher Syndrome · GrantIndex