Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey

Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey

Objective:Neonatal diabetes mellitus (NDM) may be transient or permanent, and the majority is caused by genetic mutations. Early diagnosis is essential to select the patients who will respond to oral treatment. In this investigation, we aimed to present the phenotype and genotype of our patients wit...

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Bibliographic Details
Main Authors: Yasemin Denkboy Öngen, Erdal Eren, Özgecan Demirbaş, Elif Sobu, Sian Ellard, Elisa De Franco, Ömer Tarım
Format: Article
Language:English
Published: Galenos Yayincilik 2021-03-01
Series:JCRPE
Subjects:
neonatal diabetes
genetic
sulfonylurea
monogenic diabetes
potassium channel
syndromic neonatal diabetes
Online Access: http://www.jcrpe.org/archives/archive-detail/article-preview/genotype-and-phenotype-heterogeneity-in-neonatal-d/40045

Internet

http://www.jcrpe.org/archives/archive-detail/article-preview/genotype-and-phenotype-heterogeneity-in-neonatal-d/40045

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