Literature DB >> 1721797

Prevalence of haemoglobinopathies in school children in Jordan Valley.

N Bashir1, M Barkawi, L Sharif.   

Abstract

Blood samples were drawn from 456 healthy children, 6-10 years old, to explore the prevalences of haemoglobinopathies in Northern Jordan Valley. The children were selected by the multi-stage random sampling technique. Complete blood count, haemoglobin electrophoresis and haemoglobin A2 (HbA2) estimations were carried out on all the samples. The prevalences of beta-thalassaemia minor, alpha-thalassaemia trait, sickle cell trait, and hereditary elliptocytosis were 15(3.3%), 16(3.5%), 2(0.44%) and 4(0.89%), respectively.

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Year:  1991        PMID: 1721797     DOI: 10.1080/02724936.1991.11747532

Source DB:  PubMed          Journal:  Ann Trop Paediatr        ISSN: 0272-4936


  4 in total

1.  Epidemiological profile of common haemoglobinopathies in Arab countries.

Authors:  Hanan A Hamamy; Nasir A S Al-Allawi
Journal:  J Community Genet       Date:  2012-12-08

2.  Sickle Cell Disease in Jordan: The Experience of a Major Referral Center.

Authors:  Raida I Oudat; Heba S Abualruz; Nazih Kh Abu Al-Shiek; Eman A Al-Mashaqba; Rawan A Al-Hiari; Hala A Alsoukhni; Ma'mon A Abu Hammad
Journal:  Med Arch       Date:  2021-02

Review 3.  Sickle cell disease in Middle East Arab countries.

Authors:  Mohsen A F El-Hazmi; Ali M Al-Hazmi; Arjumand S Warsy
Journal:  Indian J Med Res       Date:  2011-11       Impact factor: 2.375

Review 4.  Genetic epidemiology of hemoglobinopathies among Iraqi Kurds.

Authors:  Nasir Al-Allawi; Sarah Al Allawi; Sana D Jalal
Journal:  J Community Genet       Date:  2020-11-22
  4 in total

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