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Thalassemia Patients and Friends and thalpal Ā© A. Battaglia 2019

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Author Topic: Iron Overload In Thalassemia  (Read 3400 times)
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« on: July 31, 2011, 02:05:55 PM »

It seems genetic iron overload is "common".

East Mediterr Health J. 2011 Jun;17(6):546-51.
Role of HFE gene mutations on developing iron overload in beta-thalassaemia carriers in Egypt.
Madani HA, Afify RA, Abd El-Aal AA, Salama N, Ramy N.
SourceDepartment of Chemiakl and Clinical Pathology, University of Cairo, Cairo, Egypt. hamadani20@hotmail.com

A case-control study aimed to determine the prevalence of C282Y, H63D and S65C mutations of the HFE gene in beta-thalassaemia carriers and investigate their influence on iron absorption. A total of 41 beta-thalassaemia carriers and 40 control subjects without haemoglobinopathies were screened for the C282Y, H63D and S65C mutations by polymerase chain reaction-restriction fragment-length polymorphism. The iron status in these subjects was studied and correlated with the HFE gene mutations. H63D, S65C and C282Y allele frequencies were 30.5%, 13.4% and 7.3% respectively in beta-thalassaemia carriers and 10.0%, 2.5% and 0.0% respectively in the control group. Compound heterozygosis was found in 10 carriers (24.4%). The transferrin saturation level was high in compound heterozygote cases. Our study has shown that the HFE gene mutations are common in Egypt among beta-thalassaemia carriers compared with normal controls.

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