A case of Larsen syndrome / 대한산부인과학회지
Korean Journal of Obstetrics and Gynecology
;
: 1337-1341, 2008.
Artigo
em Coreano
| WPRIM
| ID: wpr-85233
ABSTRACT
Larsen syndrome is a rare congenital skeletal malformation (1 in 100,000 births) caused by a generalized mesenchymal connective tissue disorder. This disorder leads to a broad spectrum of anomalies. Major diagnostic criteria are multiple dislocations of large joints (especially knees), short metacarpals with cylindrical nontapering fingers and craniofacial abnormalities. Clinical variations range from mild clinical expression to lethal forms. Sporadic occurrence as well as autosomal dorminant and recessive inheritance are described.
Texto completo:
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Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Testamentos
/
Tecido Conjuntivo
/
Anormalidades Craniofaciais
/
Luxações Articulares
/
Ossos Metacarpais
/
Dedos
/
Articulações
/
Metapirileno
Idioma:
Coreano
Revista:
Korean Journal of Obstetrics and Gynecology
Ano de publicação:
2008
Tipo de documento:
Artigo
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