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Neonatal hyperinsulinism/hyperammonemia syndrome / 中国小儿急救医学
Chinese Pediatric Emergency Medicine ; (12): 583-585, 2014.
Artigo em Chinês | WPRIM | ID: wpr-455334
ABSTRACT
Neonatal hyperinsulinism/hyperammonemia syndrome is a genetic disease result from glutamate dehydrogenase gene mutations.The clinical manifestations are hypoglycemia,hyperinsulinemia and mild hyperammonemia.Hypoglycemia may occur quickly due to eating protein.It is a rare neonatal disease that was easily ignored or delayed diagnosis and treatment causing serious sequelae of nervous system.This review summarized pathogenesis,clinical manifestation and diagnosis of the disease.

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Idioma: Chinês Revista: Chinese Pediatric Emergency Medicine Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Idioma: Chinês Revista: Chinese Pediatric Emergency Medicine Ano de publicação: 2014 Tipo de documento: Artigo