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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2015
Assuntos:
Part 4: Oral/poster
Acesso em linha: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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