Neonatal diabetes mellitus due to a new KCNJ11 mutation - 10 years of the patient`s follow-up

Background. Mutations in the KCNJ11 gene, which encodes the Kir6.2 subunit of the ATP-sensitive potassium channel, often result in neonatal diabetes. Case. In this report, we describe a 10-year-old girl who is heterozygous for a new missense mutation in the KCNJ11 gene and whose treatm...

Full description

Saved in:
Bibliographic Details
Main Authors: Maja D Ješić, Helena Stock, Vera Zdravković, Smiljka Kovačević, Marko Savić, Miloš M Ješić
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2021-06-01
Series:The Turkish Journal of Pediatrics
Subjects:
Online Access:https://turkjpediatr.org/article/view/323
Tags: Add Tag
No Tags, Be the first to tag this record!