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Genetic pathogenesis and current trends in diagnosis and therapy of ATP-sensitive potassium channel congenital hyperinsulinism / 中华实用儿科临床杂志
Article em Zh | WPRIM | ID: wpr-490152
Biblioteca responsável: WPRO
ABSTRACT
ATP-sensitive potassium channel congenital hyperinsulinism (KATP-HI) is the most common and most severe type of congenital hyperinsulinism,accounting for 40%-45%.It is due to the inactivating mutations of the ABCC8 and KCNJ11 gene which encode the ATP-sensitive potassium channel.Diazoxide is the main and preferred therapy for KATP-HI.For KATP-HI children who are unresponsive to medical therapy usually need different degrees of pancreatectomy to maintain normal blood sugar level.
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Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Etiology_studies Idioma: Zh Revista: Chinese Journal of Applied Clinical Pediatrics Ano de publicação: 2016 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Etiology_studies Idioma: Zh Revista: Chinese Journal of Applied Clinical Pediatrics Ano de publicação: 2016 Tipo de documento: Article