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Cornelia de Lange Syndrome
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-97634
Biblioteca responsável: WPRO
ABSTRACT
The Cornelia de Lange syndrome is characterized by severe growth and mental retardations and a cluster of minor malformations, the facial appearance being most characteristic. In the present paper, we shall report I case of this syndrome in Korean male infant and the variability of de Lange syndrome is discussed. The bady showed hirsutism, low forehead coved with lanugo-like hair, bushy eyebrows that meet in the midline, long curely eyelashes as well as low pitched, growling cry and skeletal abnormalities of hand bones. There is no positive family history and the karyotype was normal. Although the de Lange syndrome has received more interest there is no agreement as to the possible cause.
Assuntos
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Síndrome de Cornélia de Lange / Ossos da Mão / Sobrancelhas / Pestanas / Cariótipo / Testa / Cabelo / Hirsutismo Limite: Humanos / Lactente / Masculino Idioma: Coreano Revista: Journal of the Korean Pediatric Society Ano de publicação: 1980 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Síndrome de Cornélia de Lange / Ossos da Mão / Sobrancelhas / Pestanas / Cariótipo / Testa / Cabelo / Hirsutismo Limite: Humanos / Lactente / Masculino Idioma: Coreano Revista: Journal of the Korean Pediatric Society Ano de publicação: 1980 Tipo de documento: Artigo
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