Faculty Of Pharmacy Graduation Project 2018 - 2019

Permanent URI for this collectionhttp://185.252.233.37:4000/handle/123456789/65

Browse

Browsing Faculty Of Pharmacy Graduation Project 2018 - 2019 by Subject "Genetic Diabetes"

Filter results by typing the first few letters
Now showing 1 - 1 of 1
  • No Thumbnail Available
    Item
    The association of genetic variants with the risk of type 2 diabetes mellitus in Egyptian population (RSPB2.3)
    (October University for Modern Sciences and Arts, 2019) Ateya Fahem, Madonna; Raouf Fawzy, Maged; Sabry Aziz, Michael; Ahmed Mohammed, Mirna
    Diabetes is a disorder in carbohydrate metabolism, and has no ability to produce insulin, thus maintaining appropriate levels of glucose in the blood. Insulin is secreted by beta cells that are located inside the pancreas called carrots from the role of Langerhans.its is to stimulate cells to eat glucose until cells use this sugar-generating energy. Diabetics may have dysfunctional beta cells, leading to reduced insulin secretion or insulin-resistant muscle cells because cells cannot eat glucose. In both cases it will increase glucose in the blood, causing high blood sugar. Blood glucose may accumulate and excrete excess sugar levels in the urine. Because high levels of glucose in the urine, the amount of water excreted will increase, causing high urine volume and frequent urination, as well as feeling hungry and thirsty, also sweetened with honey, "itching, weakness, weight loss. The first type of diabetes, known as insulin-dependent diabetes, usually comes in childhood Type 2 diabetes, called insulin-dependent diabetes, occurs more after the age of forty and more common with increasing age Most cases of diabetes Type II is more common than type 1 diabetes 90% of all cells are strongly linked to obesity, and diabetes is linked to the transformation of genes called KCNQ1, which plays a major role in re-polarization, which is part of the ability to work in muscle tissue. , Suggesting that this vulnerability may be behind the sensitivity to diabetes provided by the allele.The genetic mutation in SNPS (228,328 rupees and 2237,897 rupees) is caused by KCNQ1. Another gene is KCNJ11, which plays a role in the regulation of hormone secretion, for example: insulin , In beta cells. Genetic polymorphisms in this gene have been shown to be associated with increased risk of T2DM. The study is designed to detect risk factors (genetic and non-genetic) that predict the outcome of T2DM and related complications. Peripheral blood samples were collected from diabetics and natural persons. The study was conducted on 60 people. 30 control and 30 diabetes. The blood was collected after taking their consent. We will estimate the level of blood glucose and lipid form by the spectrophotometer and also use PCR technique and serialization method to determine the genetic variables in the KcnQ & KcnJ11 gene