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SQUMJ-Sultan Qaboos University Medical Journal. 2008; 8 (3): 344-346
in English | IMEMR | ID: emr-90435

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


Subject(s)
Humans , Female , Anemia, Sickle Cell/genetics , Hemoglobins, Abnormal , Hemoglobinopathies , Sickle Cell Trait/physiopathology , Anemia, Sickle Cell/physiopathology , Heterozygote , alpha-Thalassemia , Hemoglobin, Sickle
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