Journal of
Medical Laboratory and Diagnosis

  • Abbreviation: J. Med. Lab. Diagn.
  • Language: English
  • ISSN: 2141-2618
  • DOI: 10.5897/JMLD
  • Start Year: 2010
  • Published Articles: 54

Full Length Research Paper

Screening for hemoglobinipathy in Beja tribes and other minor groups living in Port Sudan City

Mohammed Omer Gibreel*,
  • Mohammed Omer Gibreel*,
  • Haematology Department, Port Sudan Ahlia College, Port Sudan, Sudan.
  • Google Scholar
Mubarak El Saeed Elkarsani
  • Mubarak El Saeed Elkarsani
  • Medical Laboratory Sciences, University of Karary, Sudan.
  • Google Scholar
Munsour Mohammed Munsoor
  • Munsour Mohammed Munsoor
  • Hematology Department, Faculty of Medical laboratory Sciences, University of Sudan, Sudan
  • Google Scholar
El Yasaa Ahmed Gubartella
  • El Yasaa Ahmed Gubartella
  • Hematology Department, Faculty of Medical laboratory Sciences, University of Sudan, Sudan
  • Google Scholar


  •  Received: 13 July 2014
  •  Accepted: 19 August 2014
  •  Published: 30 September 2014

References

Alizadeh S, Bavarsad MS, Dorgalaleh A, Khatib ZK, Dargahi H, Nassiri N, Hamid F, Rahim F, Jaseb K, Saki N (2014). Frequency of beta-thalassemia or beta-hemoglobinopathy carriers simultaneously affected with alpha-thalassemia in Iran. Clin. Lab. 60(6):941-9.
Pubmed
 
Barbara JB (2006). Haemoglobinopathy Diagnosis. Second edition, Oxford UK, Blackwell publishing pp. 70,142.
 
Bashir N, Barkawi M, Sharif L, Momani A, Gharaibeh N (1992) Prevalence of hemoglobinopathies in north Jordan. Trop. Geog. Med. 44(1-2):122-125.
Pubmed
 
Canatan D (2014). Thalassemias and Hemoglobinopathies in Turkey. Hemoglobin 17:1-3.
Crossref
 
Elderdery AY, Mills J, Mohamed BA, Cooper AJ, Mohammed AO, Eltieb N, Old J (2012). Molecular analysis of the β-globin gene cluster haplotypes in a Sudanese population with sickle cell anaemia. Int. J. Lab. Hematol. 34(3):262-266.
Crossref
 

Elderdery AY, Mohamed BA, Cooper AJ, Knight G, Mills J (2011). Tribal distribution of Haemoglobinopathies in a Sudanese patient popula-tion. J. Med. Lab. Diag. 2(4):31-37.

View

 
Firkin F, Chesterman C, Penington D, Rush B (1989) de Gruchy's Clinical Haematology in Medical practice. Fifth edition. United Kingdom, Blackwell Science. pp. 137-170.
 
Galanello R, Offit R (2010). Beta thalassaemia. Orphanet. J. Rare Dis. 5:11.
Crossref
 
Greer JP, Foerster J, Lukens JN (2003). Wintrobe's Clinical Haematology. 11th edition. London: Lippinkott Williams and Willkins publishers. p. 1019.
 
Hoffbrand AV, Catovsky D, Edward GD (2005). Postgraduate haematology. Fifth edition, Volume 1. United Kingdom, Blackwell publishing. pp. 85-103.
Crossref
 
Kaddah N, Rizk S, Kaddah AM, Salama K, Lotfy H (2009) Study of possible genetic factors determining the clinical picture of thalassemia intermedia. J. Med. Sci. 9(3)151-155.
Crossref
 
Kolita TP (2010). Guidelines for the diagnosis of the haemoglobino-pathies in Nigeria. Ann. Ibadan Postgrad. Med. 8(1):25.
 
Modell B, Khan M, Darlison M (2000). Survival in beta-thalassaemia major in the UK: data from the UK Thalassaemia Register. Lancet 355(9220):2051-2052.
Crossref
 
Mohammed AO, Attalla B, Bashir FM, Ahmed FE, El Hassan AM, Ibnauf G, Jiang W, Cavalli-Sforza LL, Karrar ZA, Ibrahim ME (2006). Relationship of the sickle cell gene to the ethnic and geographic groups populating the Sudan. Commun. Genet. 9(2):113-20.
Crossref
 
Munsoor MM, Afaf A (2011). SCT Among relatives of Sickle cell patients in Western Sudan. Can. J. Med. 2(2):20-26.
 
Nagar R, Sinha S, Raman R (2014). Haemoglobinopathies in eastern Indian states: a demographic evaluation. J. Commun. Genet. 1-8.
 
Weatherall DJ (2004). The role of molecular genetics in an evolving global health problem. Am. J. Hum. Genet. 74(3):385-392.
Crossref