Retinosis pigmentaria e hipoacusia (Síndrome de Usher)

  1. Grimaldos, P.
  2. Giménez, F.
  3. Boix, J.
  4. Alonso, L.
  5. Bosch, R.
  6. Ivorra, P.
  7. Marco, J.
Revista:
Archivos de la Sociedad Española de Oftalmologia

ISSN: 0365-6691

Ano de publicación: 1990

Volume: 59

Número: 6

Páxinas: 691-698

Tipo: Artigo

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Outras publicacións en: Archivos de la Sociedad Española de Oftalmologia

Resumo

We present eight patients suffering UsherSyndrome. We have studied their family treesand types of inheritance. Ophthalmological exploration includes: computerized perymetry and electrophysiological tests. A complete auditive and vestibular exploration was performed. The patients have been clasiffied in types 1 and 2, depending the severity of the illness. We have performed a large bibliographic revision about Usher Syndrome. Finally diffrential diagnostic of retinitis piqmentosa and hearing loss is explosed.

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