the adverse effects of pregnancies complicated by hemoglobin h (hbh) disease

Authors

maryam rabiee

jalal-aldin shams

nafiseh zafargandie

abstract

hemoglobin (hb) h disease is a moderate form of α- thalassemia resulting from various genetic defects. hbh disease is not necessarily a benign disorder as has been generally thought. we present hereby a 25- year-old iranian pregnant woman whom referred to our hospital for blood transfusion. she exhibited the clinical and hematological manifestation of hbh disease. her father carries a common α-thalassemia deletion while her mother was normal in the hematological profile. the object of this report was to provide information about pregnancies affected by hbh disease.

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Journal title:
iranian journal of pathology

Publisher: iranian society of pathology

ISSN 1735-5303

volume 10

issue 4 2015

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