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Usher Syndromes
Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL hearing loss and retinitis pigmentosa. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.
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 Macula in Usher syndrome disorders.eyes.arizona.edu |  Fundus in Usher syndrome disorders.eyes.arizona.edu |  What Is Usher Syndrome? www.ushersyndrome.nih.gov |  In Usher syndrome, the gene my.clevelandclinic.org |
 people with Usher syndrome www.nei.nih.gov |  Usher syndrome there is www.asha.org |  Type II Usher syndrome www.asha.org |  Usher syndrome - Wikipedia en.wikipedia.org |
Diagnosis and therapies
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Wikipedia
Usher syndrome, List of Gentlemen Ushers, Fimbrial usher protein, Gentleman Usher, Usher 1C, Usher of the Black Rod of the Senate of Canada, Gentleman Usher of the Blue Rod, Usher Baronets, La chute de la maison Usher (opera), CLRN1-AS1
More information
- Reported cases - Summary of cases reported on this disease.
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- WHO - World Health Organization.
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- MeSH - Medical Subject Headings.
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