Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8

Congenital hyperinsulinism (CHI) is a rare glucose metabolism disorder characterized by unregulated secretion of insulin that leads to hyperinsulinemic hypoglycemia (HH). Most cases are caused by mutations in the K(ATP)-channel genes ABCC8 and KCNJ11. We report 2 patients that experienced severe HH...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Ann Pediatr Endocrinol Metab
Main Authors: Mouron-Hryciuk, Julie, Stoppa-Vaucher, Sophie, Busiah, Kanetee, Bouthors, Thérèse, Antoniou, Maria Christina, Jacot, Eric, Brusgaard, Klaus, Christesen, Henrik Thybo, Hussain, Khalid, Dwyer, Andrew, Roth-Kleiner, Matthias, Hauschild, Michael
Formato: Artigo
Idioma:Inglês
Publicado em: Korean Society of Pediatric Endocrinology 2021
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8026340/
https://ncbi.nlm.nih.gov/pubmed/32871644
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2040042.021
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados