Literature DB >> 18654893

An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) gene.

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.

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Year:  2008        PMID: 18654893     DOI: 10.1080/03630260802173619

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  1 in total

1.  Chronic hemolytic anemia due to novel alpha-globin chain variants: critical location of the mutation within the gene sequence for a dominant effect.

Authors:  Claude Préhu; Kamran Moradkhani; Jean Riou; Michel Bahuau; Pierre Launay; Natacha Martin; Henri Wajcman; Michel Goossens; Frédéric Galactéros
Journal:  Haematologica       Date:  2009-10-08       Impact factor: 9.941

  1 in total

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