Usher syndrome: Clinical features, diagnostic options, and therapeutic prospects
Usher syndrome denotes a clinically and genetically heterogeneous combination of retinitis pigmentosa and sensorineural deafness. The division into subtypes I, II, and III is based on the degree of hearing loss: Type I is characterized by deafness from birth together with ataxia and retarded motor d...
Main Authors: | Seeliger, M, Fischer, M, Pfister, M |
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פורמט: | Journal article |
שפה: | German |
יצא לאור: |
2009
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פריטים דומים
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[Usher syndrome: clinical features, diagnostic options, and therapeutic prospects].
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יצא לאור: (2009) -
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Ushering Patients Towards Strabismus Screening in Usher’s Syndrome
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An Update on the Genetics of Usher Syndrome
מאת: José M. Millán, et al.
יצא לאור: (2011-01-01)