| Literature DB >> 26351505 |
Maryam Rabiee1, Jalal-Aldin Shams2, Nafiseh Zafargandie1.
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.Entities:
Keywords: Hemoglobin H; Iran; Pregnancy
Year: 2015 PMID: 26351505 PMCID: PMC4539740
Source DB: PubMed Journal: Iran J Pathol ISSN: 1735-5303