Comparison of diabetes phenotype in children and their mothers with permanent neonatal diabetes mellitus carrying the same KCNJ11 variants

Comparison of diabetes phenotype in children and their mothers with permanent neonatal diabetes mellitus carrying the same KCNJ11 variants

Objective. Mutations of the KCNJ11 gene are the most common cause of the permanent neonatal diabetes mellitus (PNDM). Majority of people with KNCJ11-PNDM have a de-novo mutation. We aimed to compare diabetes phenotype in two children and their mothers with PNDM carrying the same sulfonylurea-sensiti...

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Bibliographic Details
Main Authors: Stanik Juraj, Barak Lubomir, Dankovcikova Adriana, Valkovicova Terezia, Skopkova Martina, Gasperikova Daniela
Format: Article
Language:English
Published: Sciendo 2020-10-01
Series:Endocrine Regulations
Subjects:
permanent neonatal diabetes mellitus
kcnj11
children
mothers
diabetes control
sulfonylurea
c-peptide
Online Access:https://doi.org/10.2478/enr-2020-0029

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