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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Case Rep Endocrinol
मुख्य लेखकों: Morishita, Kae, Kyo, Chika, Yonemoto, Takako, Kosugi, Rieko, Ogawa, Tatsuo, Inoue, Tatsuhide
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Hindawi Publishing Corporation 2017
विषय:
ऑनलाइन पहुंच: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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