COINHERITANCE OF THALASSEMIA SYNDROMES WITH SICKLE CELL DISEASE - Abd Ali Abbas Ameen Al-Barazanchi, Zuhair;Shaker Al-Mamoori, Hind
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Sickle cell disease (SCD) is a chronic, challenging global health problem. In Iraq it is highly prevalent in two Governorates: Basra in the extreme south and Dohuk in the extreme east-north. In Basra, it represents a big burden to patients, their families and the health care system. Lot of genetic (like beta-chain haplotypes, hemoglobin (Hb) F concentration and the -thalassemia co-inheritance) and environmental factors contribute in affecting the disease behaviour.

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Produktbeschreibung
Sickle cell disease (SCD) is a chronic, challenging global health problem. In Iraq it is highly prevalent in two Governorates: Basra in the extreme south and Dohuk in the extreme east-north. In Basra, it represents a big burden to patients, their families and the health care system. Lot of genetic (like beta-chain haplotypes, hemoglobin (Hb) F concentration and the -thalassemia co-inheritance) and environmental factors contribute in affecting the disease behaviour.
Autorenporträt
Zuahir Abd Ali Abbas Al-Barazanchi Baghdad graduated College of Medicine, Mosul Univ, 1980. He served at the Medical Military services(1980-2002). Hods MSc degree in hematopathology from the Medical College Baghdad Univ., 1989 and PhD in the College of Medicine, Al-Nahrain Univ., registered as a consultant hematopatholgist.More than 30 publications