Literature DB >> 21748082

Compound heterozygosity for Hb S and Hb S-Oman: Case report.

Suresh Venugopal1, Alphonsa Shaju, Suchata Dhuri, Thuraiya Al-Harthy, Khalid B Jabal.   

Abstract

The haematological and clinical findings of a three year old Omani girl, phenotypically compound heterozygote for Hb S and Hb S Oman, are presented, further substantiated by family studies. The necessity of reviewing cases with sickle cell haemoglobin in Oman is stressed.

Entities:  

Keywords:  Abnormal haemoglobin; Case report; Haemoglobin S Disease; Haemoglobin S Oman; Haemoglobinopathies; Oman; Sickle cell anaemia; Sickle cell trait

Year:  2008        PMID： 21748082      PMCID： PMC3074849     

Source DB:  PubMed          Journal:  Sultan Qaboos Univ Med J        ISSN： 2075-051X


  3 in total

1.  A case of compound heterozygosity for Hb S and Hb S Oman.

Authors:  Raya Al Jahdhamy; Haythem Makki; Geoff Farrell; Sameer Al Azzawi
Journal:  Br J Haematol       Date:  2002-03       Impact factor: 6.998

2.  A new doubly substituted sickling haemoglobin: HbS-Oman.

Authors:  J V Langdown; D Williamson; C B Knight; D Rubenstein; R W Carrell
Journal:  Br J Haematol       Date:  1989-03       Impact factor: 6.998

3.  HbS-oman heterozygote: a new dominant sickle syndrome.

Authors:  R L Nagel; S Daar; J R Romero; S M Suzuka; D Gravell; E Bouhassira; R S Schwartz; M E Fabry; R Krishnamoorthy
Journal:  Blood       Date:  1998-12-01       Impact factor: 22.113
  3 in total

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