Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years

Congenital hyperinsulinism (CHI) caused by a glucokinase- (GCK-) activating mutation shows autosomal dominant inheritance, and its severity ranges from mild to severe. A 43-year-old female with asymptomatic hypoglycemia (47 mg/dL) was diagnosed as partial adrenal insufficiency and the administration...

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Detalles Bibliográficos
Publicado en:Case Rep Endocrinol
Main Authors: Morishita, Kae, Kyo, Chika, Yonemoto, Takako, Kosugi, Rieko, Ogawa, Tatsuo, Inoue, Tatsuhide
Formato: Artigo
Idioma:Inglês
Publicado: Hindawi Publishing Corporation 2017
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5253496/
https://ncbi.nlm.nih.gov/pubmed/28163940
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/4709262
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