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A report of 8 cases with hemoglobin H disease in an Iranian family.

Pediatric hematology and oncology - 1 Aug 2010

Azarkeivan Azita, Azita Azarkeivan, Neishabury Maryam, Hadavi Valeh, Esteghamat Fatemehsadat, Fatemehsadat Esteghamat, Enrahimkhani Saideh, Najmabadi Hossein, Hossein Najmabadi

Abstract excerpt

alpha-Thalassemia is a common genetic disorder in Iran. However, no comprehensive data on epidemiology of severe forms of alpha-thalassemia, including hemoglobin H (HbH) or hydrops fetalis, is available in this population. This is a first case report of an Iranian family with large number of HbH individuals. The proband is a 48-year-old woman, referred to our center with anemia and no history of previous blood...

Topics

DNA Mutational Analysis
Family
Female
Genetic Testing
Genotype
Hemoglobin H
Humans
Hydrops Fetalis
Iran
Middle Aged
Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Pregnancy

Prenatal Diagnosis

alpha-Thalassemia

Source

Identifiers

PMID: 20670167
DOI: 10.3109/08880010903536201

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