Retinosis pigmentaria e hipoacusia (Síndrome de Usher)
- Grimaldos, P.
- Giménez, F.
- Boix, J.
- Alonso, L.
- Bosch, R.
- Ivorra, P.
- Marco, J.
ISSN: 0365-6691
Argitalpen urtea: 1990
Alea: 59
Zenbakia: 6
Orrialdeak: 691-698
Mota: Artikulua
Beste argitalpen batzuk: Archivos de la Sociedad Española de Oftalmologia
Laburpena
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.