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 |
---|---|
Format: | Journal article |
Sprog: | German |
Udgivet: |
2009
|
Lignende værker
-
[Usher syndrome: clinical features, diagnostic options, and therapeutic prospects].
af: Seeliger, M, et al.
Udgivet: (2009) -
Usher syndrome: clinical features, molecular genetics and advancing therapeutics
af: Maria Toms, et al.
Udgivet: (2020-09-01) -
Usher Syndrome
af: Alessandro Castiglione, et al.
Udgivet: (2022-01-01) -
Ushering Patients Towards Strabismus Screening in Usher’s Syndrome
af: Tanvi Shetty, et al.
Udgivet: (2024-09-01) -
An Update on the Genetics of Usher Syndrome
af: José M. Millán, et al.
Udgivet: (2011-01-01)