Novel GLIS3 mutation in patient with neonatal diabetes mellitus and congenital hypothyroidism (NDH-syndrome)

Mutations in the GLIS3 gene encoding the GLIS3 transcription factor are cause of a rare syndromic form of neonatal diabetes mellitus (NDM) with congenital hypothyroidism. Additional features include congenital glaucoma, hepatic fibrosis, polycystic kidneys, developmental delay and other anomalies. T...

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Bibliographic Details
Main Authors:	Yu. V. Tikhonovich, L. G. Chernich, I. N. Velikanov, V. M. Polyakova, E. V. Vasilyev, V. M. Petrov, E. V. Shreder, Е. V. Glavatskich, A. N. Tyulpakov
Format:	Article
Language:	English
Published:	Endocrinology Research Centre 2022-03-01
Series:	Сахарный диабет
Subjects:	neonatal diabetes mellitus gene glis3 ndh-syndrome congenital hypothyroidism
Online Access:	https://www.dia-endojournals.ru/jour/article/view/12826
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Novel GLIS3 mutation in patient with neonatal diabetes mellitus and congenital hypothyroidism (NDH-syndrome)

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