Homozygous Insulin Promotor Gene Mutation Causing Permanent Neonatal Diabetes Mellitus and Childhood Onset Autoantibody Negative Diabetes in the Same Family

PURPOSE: To report a family with a homozygous INS promotor gene mutation causing permanent neonatal diabetes mellitus (PNDM) in one sibling and autoantibody negative childhood onset diabetes in another sibling. CASE PRESENTATION: Patient 1 is a 12-year-old girl born at term with low birth weight to...

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Detalles Bibliográficos
Autores principales: Haris, Basma, Mohammed, Idris, Al-Khawaga, Sara, Hussain, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819275/
https://www.ncbi.nlm.nih.gov/pubmed/35140529
http://dx.doi.org/10.2147/IMCRJ.S349424

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819275/
https://www.ncbi.nlm.nih.gov/pubmed/35140529
http://dx.doi.org/10.2147/IMCRJ.S349424

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