Genetic Susceptibility to Transient and Permanent Neonatal Diabetes Mellitus | ||
| Journal of Pediatric Perspectives | ||
| مقاله 10، دوره 3، شماره 6.1، بهمن 2015، صفحه 1073-1081 اصل مقاله (889.43 K) | ||
| شناسه دیجیتال (DOI): 10.22038/ijp.2015.5628 | ||
| نویسندگان | ||
| Masoud Dehghan Tezerjani1؛ Mohammad Yahya Vahidi Mehrjardi2؛ Seyed Mehdi Kalantar1؛ Mohammadreza Dehghani* 2 | ||
| 1Reproductive and Genetic Unit, Yazd Research and Clinical center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran | ||
| 2Medical 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. | ||
| کلیدواژهها | ||
| TNDM؛ PNDM؛ Neonatal diabetes؛ mutations | ||
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