Literature DB >> 2807263

Glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in the Ok Tedi impact region of Papua New Guinea.

G J Schuurkamp, K K Bhatia, R K Kereu, P K Bulungol.   

Abstract

We report the distribution of two genetic traits, glucose-6-phosphate dehydrogenase (G-6-PD) deficiency and hereditary ovalocytosis (HO) in a number of populations living in the Ok Tedi impact region of Papua New Guinea. Significant interpopulation heterogeneity in the distributions of G-6-PD deficiency and HO was observed. The highlands populations of the region did not show any G-6-PD deficiency, but in the highlands fringe and lowland populations the trait has achieved polymorphic frequencies. Hereditary ovalocytosis is significantly more common in the region and is present in all the populations studied, including those in the highland valleys. Distribution patterns of the two genetic markers correspond well with the pattern of malaria endemicity in the region, providing support for the hypothesis that relates the distribution of these polymorphisms to that of malaria.

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Year:  1989        PMID: 2807263

Source DB:  PubMed          Journal:  Hum Biol        ISSN: 0018-7143            Impact factor:   0.553


  1 in total

1.  Accurate light microscopic diagnosis of South-East Asian ovalocytosis.

Authors:  Christian P Nixon; Ari W Satyagraha; Grayson L Baird; Alida R Harahap; Lydia V Panggalo; Lenny L Ekawati; Inge Sutanto; Din Syafruddin; J Kevin Baird
Journal:  Int J Lab Hematol       Date:  2018-07-13       Impact factor: 2.877

  1 in total

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