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

• Asıl Yazarlar: Alexandru-Ștefan Niculae (Yazar), Claudia Bolba (Yazar), Alina Grama (Yazar), Alexandra Mariş (Yazar), Laura Bodea (Yazar), Simona Căinap (Yazar), Alexandra Mititelu (Yazar), Otilia Fufezan (Yazar), Tudor Lucian Pop (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: MDPI AG, 2023-10-01T00:00:00Z.
• Konular: article
• Online Erişim: 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...