AB076. Congenital hyperinsulinism due to mutation of HNF4A: a case report

BACKGROUND: Hyperinsulinemic hypoglycemia (HH) is the commonest cause of persistent hypoglycemia in the neonatal and infancy periods. HNF4A mutations are the third most common cause of diazoxide responsive congenital hyperinsulinism. Individuals carrying HNF4A mutations that result in familial monog...

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Foilsithe in:Ann Transl Med
Main Authors: Duong, Dang Anh, Dung, Vu Chi, Dat, Nguyen Phu, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dien, Tran Minh
Formáid: Artigo
Teanga:Inglês
Foilsithe: AME Publishing Company 2015
Ábhair:
Part 4: Oral/poster
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563400/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB076
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