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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Detalles Bibliográficos
Autores principales: Niculae, Alexandru-Ștefan, Bolba, Claudia, Grama, Alina, Mariş, Alexandra, Bodea, Laura, Căinap, Simona, Mititelu, Alexandra, Fufezan, Otilia, Pop, Tudor Lucian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594453/
https://www.ncbi.nlm.nih.gov/pubmed/37873802
http://dx.doi.org/10.3390/pediatric15040056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594453/
https://www.ncbi.nlm.nih.gov/pubmed/37873802
http://dx.doi.org/10.3390/pediatric15040056

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