genetic susceptibility to transient and permanent neonatal diabetes mellitus

نویسندگان

masoud dehghan tezerjani reproductive and genetic unit, yazd research and clinical center for infertility, shahid sadoughi university of medical sciences, yazd, iran

mohammad yahya vahidi mehrjardi medical genetic research center, shahid sadoughi university of medical sciences, yazd, iran

seyed mehdi kalantar reproductive and genetic unit, yazd research and clinical center for infertility, shahid sadoughi university of medical sciences, yazd, iran

mohammadreza dehghani medical genetic research center, shahid sadoughi university of medical sciences, yazd, iran

چکیده

neonatal diabetes mellitus (ndm) is a rare kind of diabetes characterized by hyperglycemia and low levels of insulin. clinically, it is categorized into two main types: transient ndm (tndm) and permanent ndm (pndm). these types are diagnosed based on duration of insulin dependence early in the disease. in tndm, diabetes begins in the first few weeks of life with remission in a few months. however, infant with pndm have insulin secretory failure in the late fetal or early post-natal period with no remission. mutation in the kcnj11 and abcc8 genes can cause both tndm and pndm, and infant with this mutation can respond to transition from insulin to sulfonylureas making identification of genes involved in the disease important for appropriate treatment.

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Genetic Susceptibility to Transient and Permanent Neonatal Diabetes Mellitus

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عنوان ژورنال:
international journal of pediatrics

جلد ۳، شماره ۶.۱، صفحات ۱۰۷۳-۱۰۸۱

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