Estimation of the prevalence of Hemoglobinopathies in Erbil governorate, Kurdistan region of Iraq

BACKGROUND: Thalassemia syndromes and structural hemoglobin variants generate blood crisis of variable clinical symptoms, ranging from mild-to-moderate hematological disorder to severe, lifelong, transfusion-dependent anemia. The aim of current study was to uncover the prevalence of thalassemia and...

Descripció completa

Dades bibliogràfiques

Autors principals:	Sarkar S Aziz, Bahra K Hamad, Hero O Hamad, Muzhda I Qader, Eman N Ali, Rayan H Muhammed, Mudhir Sabir Shekha
Format:	Artigo
Idioma:	Inglês
Publicat:	Wolters Kluwer Medknow Publications 2022-01-01
Col·lecció:	Iraqi Journal of Hematology
Matèries:	erbil hemoglobin hemoglobinopathies prevalence sickle cell disorder thalassemia
Accés en línia:	http://www.ijhonline.org/article.asp?issn=2072-8069;year=2022;volume=11;issue=1;spage=19;epage=24;aulast=Aziz
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!