Literature DB >> 469897

Inherited anaemias in the Greek community of Cape Town.

R P Bonafede, M C Botha, P Beighton.   

Abstract

Cape Town has a Greek community of about 5000, of whom approximately 75% originate from the island of Lesbos. In a survey of inherited haematological conditions in this population, 250 unrelated volunteers were investigated. The prevalence of heterozygous beta-thalassaemia was found to be 6.4%, with a gene frequency of 0.033. G6PD deficiency was detected in 10 males and it can be estimated that the prevalence in the male members of this population is 6.7%, with a gene frequency of 0.067. Hereditary spherocytosis was found in three respondents and this represents a prevalence of 1.2%, with a gene frequency of 0.006. One subject was heterozygous for the sickle cell trait (HbS) and another volunteer had haemoglobin Lepore, which had already been diagnosed in Greece. Our findings with respect to beta-thalassaemia and G6PD deficiency are similar to those reported from regions in Greece where malaria is not highly endemic.

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Year:  1979        PMID: 469897      PMCID: PMC1012690          DOI: 10.1136/jmg.16.3.197

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  8 in total

1.  THALASSAEMIA, GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, SICKLING, AND MALARIAL ENDEMICITY IN GREECE: A STUDY OF FIVE AREAS.

Authors:  G STAMATOYANNOPOULOS; P FESSAS
Journal:  Br Med J       Date:  1964-04-04

2.  The methemoglobin reduction test for primaquine-type sensitivity of erythrocytes. A simplified procedure for detecting a specific hypersusceptibility to drug hemolysis.

Authors:  G J BREWER; A R TARLOV; A S ALVING
Journal:  JAMA       Date:  1962-05-05       Impact factor: 56.272

3.  Metabolic polymorphisms and the role of infectious diseases in human evolution.

Authors:  A G MOTULSKY
Journal:  Hum Biol       Date:  1960-02       Impact factor: 0.553

4.  Solubilities of naturally occurring mixtures of human hemoglobin.

Authors:  H A ITANO
Journal:  Arch Biochem Biophys       Date:  1953-11       Impact factor: 4.013

5.  Types of thalassaemia-trait carriers as revealed by a study of their incidence in Greece.

Authors:  B MALAMOS; P FESSAS; G STAMATOYANNOPOULOS
Journal:  Br J Haematol       Date:  1962-01       Impact factor: 6.998

6.  Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors:  K SINGER; A I CHERNOFF; L SINGER
Journal:  Blood       Date:  1951-05       Impact factor: 22.113

7.  Prevalence of beta0 and beta+ thalassemia genes in Greek children with homozygous beta-thalassemia.

Authors:  C Kattamis; K Karambula; A Metaxotou-Mavromati; V Ladis; A Constantopoulos
Journal:  Hemoglobin       Date:  1978       Impact factor: 0.849

8.  Antenatal diagnosis of thalassaemia major.

Authors:  D V Fairweather; B Modell; V Berdoukas; B P Alter; D G Nathan; D Loukopoulos; W Wood; J B Clegg; D J Weatherall
Journal:  Br Med J       Date:  1978-02-11
  8 in total

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