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Distribution of β‐thalassemia trait and erythrocyte glucose‐6‐phosphate dehydrogenase deficiency in the Markham river valley of New Guinea

Bibliographic Data

ID8317676
AuthorsEugene Giles (Harvard University), Cyril C Curtain (0000-0001-6955-320X, Harvard University), A Baumgarten (Harvard University)
Year1967
Volume27
Issue1
Pages83-88
Publication date1967-07-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueAmerican Journal of Physical Anthropology (JOURNAL)
Journal identifiersISSN: 0002-9483 • E-ISSN: 1096-8644
PublisherWiley (PUBLISHER • GB)
DOI10.1002/ajpa.1330270110
PMID6058057
OpenAlexW1973482141
LanguageEN
Citations received4
References cited9

Ten villages in or near the Markham Valley, northeastern New Guinea, have provided a sample of 476 males for the ascertainment of glucose‐6‐phosphate dehydrogenase (G6PD) deficiency and 810 individuals of both sexes for the investigation of the β‐thalassemia trait. An extreme heterogeneity was found in the prevalence of both traits when the villages were analyzed separately (from 1.5% to 18.2% demonstrating G6PD deficiency and from 0 to 22.8% evincing β‐thalassemia trait). The latter result counters an earlier report from the same region that β‐thalassemia trait frequencies correlated negatively with altitude and (presumably) positively with endemicity of malaria. The present findings, based on a more representative sample, do not necessarily invalidate the relationship between malaria and β‐thalassemia trait suggested by earlier studies, but they do make clear that correlation in New Guinea, at least, may be complicated by random genetic drift, although other possibilities are discussed. The heterogeneous distribution of G6PD deficiency in the present study confirms similar earlier findings. The importance of sample provenience and anthropological data in the interpretation of differences in the distribution of genetically determined traits is stressed

Biology · Dehydrogenase · Disease · Evolutionary biology · Glucose-6-phosphate dehydrogenase · Glucose-6-phosphate dehydrogenase deficiency · Glucosephosphate Dehydrogenase Deficiency · Malaria · Sickle cell trait · Thalassemia · Trait · Biochemistry · Demography · Endocrinology · Genetics · Hemoglobinopathies and Related Disorders · Immunology · Internal Medicine · Iron Metabolism and Disorders · Medicine · Neonatal Health and Biochemistry

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    Open Access•Marcus S Goldstein•American Journal of Physical…•1969

  • The ethnological significance of the gamma‐globulin (Gm) factors in Melanesia

    Open Access•Cyril C Curtain, Erna van Loghem et al.•American Journal of Physical…•1971

  • The distribution of haptoglobin and transferrin types in northeast New Guinea

    Open Access•A Baumgarten, Eugene Giles et al.•American Journal of Physical…•1968

  • Human Genetics, Paleoenvironments, and Malaria

    Open Access•Jeffrey T Clark, Kevin M Kelly•American Anthropologist•1993

  • Contribution of red cell enzyme deficiency trait to an understanding of genetic relationships between Melanesian and other populations

    Open Access•Chev Kidson, J G Gorman•American Journal of Physical…•1962

  • A blood group genetical survey in New Britain

    Open Access•R T Simmons, D Carleton Gajdusek et al.•American Journal of Physical…•1960

  • Distribution pattern, population genetics and anthropological significance of thalassemia and abnormal hemoglobins in Melanesia

    Open Access•Cyril C Curtain, Chev Kidson et al.•American Journal of Physical…•1962

  • Distribution pattern of an inherited trait, red cell enzyme deficiency, in New Guinea and New Britain

    Open Access•J G Gorman, Chev Kidson•American Journal of Physical…•1962

Unique citing works4
Citations per year0,07
Citation span1968 - 1993 (26)
Citation velocityhistorical
Highly citedNo
Citation typesNeutral: 4

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