| Literature DB >> 18654893 |
Kamran Moradkhani1, Elodie Mazurier, Piero C Giordano, Henri Wajcman, Claude Préhu.
Abstract
In a family of Spanish origin, five individuals presented a heterozygous alpha(0)-thalassemia (alpha-thal)-like phenotype. All had a -alpha(3.7) deletion with the recombinant alpha gene carrying the Hb Suan-Dok [alpha109(G16)LeuArg] mutation, proposed to be thalassemic. Thus, the abnormal chromosome carried an alpha(0)-thal-like allele that has to be taken into account for genetic counseling and prenatal diagnosis. The possibility of Hb H disease or hydrops fetalis should be considered when this allele is associated with alpha(+)-thal or with another alpha(0)-thal, respectively. Other described genotypes associated with Hb Suan-Dok are discussed.Entities:
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Year: 2008 PMID: 18654893 DOI: 10.1080/03630260802173619
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849