Literature DB >> 3609256

Alpha-thalassaemia in Nigeria: its interaction with sickle-cell disease.

A G Falusi, G J Esan, H Ayyub, D R Higgs.   

Abstract

We have determined the molecular basis and frequency of alpha-thalassaemia in Nigeria. The alpha-thalassaemia determinant in this population is caused by only one type of single alpha globin gene deletion (-alpha 3.7). Comparison of the haematological features of those patients who have sickle-cell disease with (-alpha/alpha alpha, -alpha/-alpha) or without (alpha alpha/alpha alpha) alpha-thalassaemia showed similar trends to those reported in Jamaican and U.S. patients with these interactions. However, in contrast to studies in some other African populations we have shown that the frequency of alpha-thalassaemia in Nigeria is the same (0.24) in patients with or without homozygous sickle-cell disease (AA, AS and AC genotypes).

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Year:  1987        PMID: 3609256     DOI: 10.1111/j.1600-0609.1987.tb00013.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  8 in total

1.  Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.

Authors:  Irene Lubega; Christopher M Ndugwa; Edison A Mworozi; James K Tumwine
Journal:  Afr Health Sci       Date:  2015-06       Impact factor: 0.927

2.  Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia.

Authors:  Oladele S Olatunya; Dulcineia M Albuquerque; Adekunle Adekile; Fernando F Costa
Journal:  J Clin Lab Anal       Date:  2018-08-20       Impact factor: 2.352

Review 3.  Differences in the clinical and genotypic presentation of sickle cell disease around the world.

Authors:  Santosh L Saraf; Robert E Molokie; Mehdi Nouraie; Craig A Sable; Lori Luchtman-Jones; Gregory J Ensing; Andrew D Campbell; Sohail R Rana; Xiao M Niu; Roberto F Machado; Mark T Gladwin; Victor R Gordeuk
Journal:  Paediatr Respir Rev       Date:  2013-11-15       Impact factor: 2.726

4.  Multiple complications in a sickle cell disease patient: a case report.

Authors:  J A Olaniyi
Journal:  Clin Med Case Rep       Date:  2008-07-08

5.  HAEMATOLOGICAL PROFILE AND BLOOD TRANSFUSION PATTERN OF PATIENTS WITH SICKLE CELL ANAEMIA VARY WITH SPLEEN SIZE.

Authors:  F A Fasola; A J Adekanmi
Journal:  Ann Ib Postgrad Med       Date:  2019-06

6.  The Effect of Alpha Thalassemia, HbF and HbC on Haematological Parameters of Sickle Cell Disease Patients in Ibadan, Nigeria.

Authors:  Foluke Atinuke Fasola; Oluwatoyin Aduke Babalola; Biobele Jotham Brown; Abayomi Odetunde; Adeyinka Gladys Falusi; Olufunmilayo Olopade
Journal:  Mediterr J Hematol Infect Dis       Date:  2022-01-01       Impact factor: 2.576

Review 7.  Thalassaemia is a tropical disease.

Authors:  T R Kotila
Journal:  Ann Ib Postgrad Med       Date:  2012-12

8.  Guidelines for the diagnosis of the haemoglobinopathies in Nigeria.

Authors:  Taiwo R Kotila
Journal:  Ann Ib Postgrad Med       Date:  2010-06
  8 in total

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