Literature DB >> 11146568

Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA].

C L Harteveld1, J Traeger-Synodinos, A Ragusa, M Fichera, E Kanavakis, C Kattamis, P Giordano, G Schilirò, L F Bernini.   

Abstract

BACKGROUND AND OBJECTIVES: The occurrence of Hb CS is usually limited to the geographic area which includes Southern China and South East Asia. In 1968 Hb CS was also found to occur in the Mediterranean area where it was originally described as Hb Athens. We investigated the independent origin of these termination codon mutations of the alpha 2-globin gene by determining the alpha-cluster haplotype and comparing the hematologic data from Hb CS-Hb H patients and their family members. DESIGN AND METHODS: We studied one Hb CS-Hb H patient of Greek origin and a Sicilian family in which one individual was affected by Hb CS-Hb H. The haplotype of the Hb CS allele was determined and compared to the haplotype of an Hb CS-Hb H individual of Chinese origin.
RESULTS: The haplotype found for the Greek and Sicilian Hb CS was the same but differed significantly from the Asiatic Hb CS mutation. INTERPRETATION AND
CONCLUSIONS: The Hb CS mutation found in both Mediterranean patients arose independently in the Mediterranean area. The difference in clinical manifestation of the Hb CS-Hb H disease in both patients is less common but consistent with similar variation in the clinical expression of analogous Hb Icaria-Hb H disease patients.

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Year:  2001        PMID: 11146568

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  3 in total

1.  Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis.

Authors:  Wittaya Jomoui; Goonnapa Fucharoen; Kanokwan Sanchaisuriya; Van Hoa Nguyen; Supan Fucharoen
Journal:  PLoS One       Date:  2015-12-18       Impact factor: 3.240

2.  Role of α-globin H helix in the building of tetrameric human hemoglobin: interaction with α-hemoglobin stabilizing protein (AHSP) and heme molecule.

Authors:  Elisa Domingues-Hamdi; Corinne Vasseur; Jean-Baptiste Fournier; Michael C Marden; Henri Wajcman; Véronique Baudin-Creuza
Journal:  PLoS One       Date:  2014-11-04       Impact factor: 3.240

3.  Molecular Basis of α-Thalassemia in Iran

Authors:  Atefeh Valaei; Morteza Karimipoor; Alireza Kordafshari; Sirous Zeinali
Journal:  Iran Biomed J       Date:  2018-01-01
  3 in total

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