Wolcott-Rallison Syndrome, a Rare Cause of Permanent Diabetes Mellitus in Infants-Case Report

Wolcott-Rallison syndrome is a rare cause of permanent neonatal diabetes mellitus caused by mutations in the eukaryotic translation initiation factor 2 alpha kinase 3 gene (EIF2AK3). Individuals affected by this disorder have severe hyperglycemia, pancreatic failure, and bone abnormalities and are p...

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Veröffentlicht in:	Pediatric reports 2023, Vol.15 (4), p.608-616
Hauptverfasser:	Niculae, Alexandru-Ștefan, Bolba, Claudia, Grama, Alina, Mariş, Alexandra, Bodea, Laura, Căinap, Simona, Mititelu, Alexandra, Fufezan, Otilia, Pop, Tudor Lucian
Format:	Report
Sprache:	eng
Online-Zugang:	Volltext
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