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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.


Keywords

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

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How to Cite
Venugopal, S., Shaju, A., Dhuri, S., Al-Harthy, T., & Jabal, K. B. (2008). Compound heterozygosity for Hb S and Hb S-Oman : Case report. Sultan Qaboos University Medical Journal, 8(3), 344–346. Retrieved from https://journals.squ.edu.om/index.php/squmj/article/view/1384

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