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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Case Rep Endocrinol
Autors principals: Morishita, Kae, Kyo, Chika, Yonemoto, Takako, Kosugi, Rieko, Ogawa, Tatsuo, Inoue, Tatsuhide
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2017
Matèries:
Case Report
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars