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...
Salvato in:
| Autori principali: | , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Pediatric Endocrinology and Diabetes Society
2023-12-01
|
| Serie: | JCRPE |
| Soggetti: | |
| Accesso online: | https://jcrpe.org/jvi.aspx?un=JCRPE-44127&volume=15&issue=4 |
| Tags: |
Nessun Tag, puoi essere il primo ad aggiungerne!!
|