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JBMS-Journal of the Bahrain Medical Society. 1996; 8 (2): 117-119
in English | IMEMR | ID: emr-41225

ABSTRACT

A rare combination of haemoglobin-S and haemoglobin-H disease was observed in a Bahraini woman during her pregnancy. She had presented with anaemia not responding to usual haematenics. The haematological and genetic studies suggested haemoglobin-H most likely to be due to non deletional type of alpha thalassemia, which is different from deletional variants present in other parts of the world


Subject(s)
Hemoglobin H , Hemoglobinopathies
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