عنوان المقالة: The Effect of Iron Overload on the Function of Some Endocrine Glands in β-Thalassemia Major Patients.
منال فرحان محسن الخاقاني | Dr. Manal F. Alkhaqani | 3921
Publication Type
Journal
Arabic Authors
English Authors
HK Al-Hakeim, MM Al-Khaqani
Abstract
Thalassemia is a term that refers to a group of genetic disorders characterized by a defect in the synthesis of hemoglobin. It is sometimes called Mediterranean anemia. Many biochemical changes in the blood accompany this disease. In this research, some biochemical parameters were measured in thalassemic patients and compared with healthy control group. These parameters include Serum iron, TIBC, were measured Spectrophotometrically. Serum ferritin, Iisulin, GH, Testosterone, T3, T4, TSH, Cortisol, & Prolactine were measured by ELISA technique. The results have revealed a moderate state of iron overload in the thalassemia patients. Furthermore, there is a decrease in the level of serum cortisol, T4, prolactine and pancreatic beta cell function percentage (HOMA% B) in thalassemic while serum TSH level is higher in thalassemic patients in comparing with control group. The changes in the hormone levels …
Publication Date
2/1/2013
Publisher
Al-Kufa University Journal for Biology
Volume No
5
Issue No
ISSN/ISBN
2
Pages
104-123
External Link
https://www.iasj.net/iasj?func=article&aId=82088
Keywords
Thalassemia --- Mediterranean anemia --- measured Spectrophotometrically --- Serum ferritin --- Iisulin --- GH --- Testosterone --- T3 --- T4 --- TSH --- Cortisol --- & Prolactine -
رجوع