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

• Main Authors: Alexandru-Ștefan Niculae (Author), Claudia Bolba (Author), Alina Grama (Author), Alexandra Mariş (Author), Laura Bodea (Author), Simona Căinap (Author), Alexandra Mititelu (Author), Otilia Fufezan (Author), Tudor Lucian Pop (Author)
• Format: Book
• Published: MDPI AG, 2023-10-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...