Concept information
Término preferido
Usher Syndromes
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Tipo
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mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Deafness-Retinitis Pigmentosa Syndrome
- Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
- Graefe-Usher Syndrome
- Hallgren Syndrome
- Retinitis Pigmentosa-Deafness Syndrome
- Usher Syndrome
- Usher's Syndrome
En otras lenguas
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francés
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Syndrome d'Usher
-
Syndromes de Usher
URI
http://data.loterre.fr/ark:/67375/JVR-C18VLX29-5
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