Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation

Neonatal diabetes and congenital hypothyroidism (CH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the GLIS3 gene. Small for gestational age, congenital glaucoma, polycystic kidney disease, cholestatic hepatic fibrosis, pancreatic exocrine insufficiency, dev...

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Bibliographic Details
Published in:JCRPE
Main Authors: Emre Sarıkaya, Mustafa Kendirci, Mikail Demir, Munis Dündar
Format: Article
Language:English
Published: Pediatric Endocrinology and Diabetes Society 2023-12-01
Subjects:
glis3
neonatal diabetes
congenital hypothyroidism
congenital glaucoma
Online Access:https://jcrpe.org/jvi.aspx?un=JCRPE-44127&volume=15&issue=4

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