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   genetic susceptibility to transient and permanent neonatal diabetes mellitus  
   
نویسنده dehghan tezerjani masoud ,vahidi mehrjardi mohammad yahya ,kalantar mehdi ,dehghani mohammadreza
منبع journal of pediatric perspectives - 2015 - دوره : 3 - شماره : 6-1 - صفحه:1073 -1081
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 postnatal 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.
کلیدواژه tndm ,pndm ,neonatal diabetes ,mutations
آدرس yazd shahid sadoghi university of medical sciences, yazd research and clinical center for infertility, reproductive and genetic unit, ایران, yazd shahid sadoghi university of medical sciences, medical genetic research center, ایران, yazd shahid sadoghi university of medical sciences, yazd research and clinical center for infertility, reproductive and genetic unit, ایران, yazd shahid sadoghi university of medical sciences, medical genetic research center, ایران
پست الکترونیکی mrezdehghani@gmail.com
 
     
   
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