Artigo Acesso aberto

Usher's and Hallgren's Syndromes

1974; Cambridge University Press; Volume: 23; Issue: S1 Linguagem: Inglês

10.1017/s1120962300023623

ISSN

2059-6316

Autores

S. Merin, F.A. Abraham, E. Auerbach,

Tópico(s)

Retinal Development and Disorders

Resumo

A study has been made of 35 patients belonging to 20 families, all diagnosed as Usher's syndrome (retinitis pigmentosa and deafness). The results indicate that there are four clinical types, which have been called Types I to IV. Genetically, they represent at least two, and possibly three or four, separate entities.

Referência(s)