Seven hereditary syndromes with pigmentary retinopathy. A review and differential diagnosis.
Clin Pediatr (Phila)
; 24(10): 578-83, 1985 Oct.
Article
em En
| MEDLINE
| ID: mdl-3896611
ABSTRACT
This article reviews several autosomal recessive syndromes characterized by pigmentary retinopathy and, in many, combined with deafness, hypogonadism, and/or mental retardation. These syndromes are manifested in infancy and childhood. Although no specific treatment is available, an early diagnosis can be the first step in initiating symptomative management and preventive measures for the patient and family.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Retinose Pigmentar
/
Doenças Genéticas Inatas
Tipo de estudo:
Diagnostic_studies
/
Screening_studies
Limite:
Female
/
Humans
/
Male
Idioma:
En
Ano de publicação:
1985
Tipo de documento:
Article