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العنوان
Study of Exon13 Mutations of The Insulin Receptor Gene by DNA Sequencing in Type II Diadetic Patients /
المؤلف
Gamal Eldeen, Sarah Hamed Mohammed.
هيئة الاعداد
باحث / ساره حامد محمد جمال الدين
مشرف / ثريا السيد بدوى
مشرف / امل حلمى عبد الحميد مصطفى
مشرف / لؤى محمد مبروك الاحول
مشرف / لا يوجد
الموضوع
Clinical Pathology.
تاريخ النشر
2017.
عدد الصفحات
p 146. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
علم الأعصاب السريري
تاريخ الإجازة
19/7/2017
مكان الإجازة
جامعة طنطا - كلية الطب - الباثولوجيا الاكلينيكيه
الفهرس
Only 14 pages are availabe for public view

from 179

from 179

Abstract

Type 2 diabetes mellitus is a chronic progressive disease and the most common form of diabetes mellitus,it results from an imbalance between insulin sensitivity and insulin secretion.Glucose production fails to be regulated adequately by insulin, leading to hepatic glucose overproduction and diminished glucose uptake by muscle tissue.Obesity is the most frequently encountered metabolic disease worldwide.Moreover, its incidence and prevalence are rising rapidly. It is generally considered to be a strong risk for the later development of Type 2 diabetes mellitus as it can cause increased insulin resistance.The insulin receptor is usually expressed at low levels in all cell types except in insulin target tissues where insulin receptor is expressed at a very high level. The identification of genetic defects in human insulin receptor gene that are associated with extreme insulin resistance and glucose intolerance has provided insight into the possible role of the human insulin receptor gene in the development of non-insulin dependent diabetes mellitus The aim of this study was to identify any mutations in exon 13 of the insulin receptor gene by DNA sequencing which may cause insulin resistance in a group of Egyptian patients with type II DM and compare the obtained results to that reported in other populations.