A Case of Laurence-Moon-Biedl Syndrome
Journal of the Korean Ophthalmological Society
;
: 671-674, 1989.
Artigo
em Coreano
| WPRIM
| ID: wpr-135976
ABSTRACT
Laurence-Moon-Biedl syndrome is a rare and autosomal recessive disorder characterized by obesity, hypogenitalism, polydactylism, mental retardation and retinitis pigmentosa. Occasionally, this syndrome is accompanied by nystagmus, cataract, syndactylism, microcephaly, oxycephaly and congenital heart diseases. Recently, the authors have experienced a 20-year-old male patient who has retinitis pigmentosa, pendular nystagmus, obesity, hypogenitalism, polydactylism, mental retardation and gynecomastia. We report a case of Laurence-Moon-Biedl syndrome with the review of literature.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Catarata
/
Retinose Pigmentar
/
Nistagmo Patológico
/
Polidactilia
/
Craniossinostoses
/
Ginecomastia
/
Cardiopatias
/
Síndrome de Laurence-Moon
/
Deficiência Intelectual
/
Microcefalia
Limite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1989
Tipo de documento:
Artigo
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