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...
Main Authors: | Emre Sarıkaya, Mustafa Kendirci, Mikail Demir, Munis Dündar |
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Format: | Article |
Language: | English |
Published: |
Galenos Yayincilik
2023-12-01
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Series: | JCRPE |
Subjects: | |
Online Access: | https://jcrpe.org/jvi.aspx?un=JCRPE-44127&volume=15&issue=4 |
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