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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...
Autores principales: | Haris, Basma, Mohammed, Idris, Al-Khawaga, Sara, Hussain, Khalid |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
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 |
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