Phenotype: Hemolytic anemia due to G6PD deficiency (Glucose-6-phosphate dehydrogenase deficiency)


OMIM: 300908
Inheritance: X-linked recessive
Classification: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

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G6PD || c.563C>T

Gene/Locus:    G6PD
Dna Change:    c.563C>T
Protein Change:    p.Ser188Phe
Mutation Type:   
Mutation Effect:   
Location:    Exon 6
Transcript:    NM_001042351.1

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
ItalyNANA69% (allele frequency)NAMartinez di Montemuros F et al., 1997Martinez di Montemuros F, Dotti C, Tavazzi D, Fiorelli G, Cappellini MD, . Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy.. Haematologica. 1997; 82(4):440-5
TunisiaNANA3 patients/ 41 unrelated patients (11 females and 30 males)NADaoud BB et al., 2008Daoud BB, Mosbehi I, Préhu C, Chaouachi D, Hafsia R, Abbes S, . Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia.. Pathol. Biol.. 2008; 56(5):260-7
TurkeyNANA80% (40 patients /50 unrelated male subjects)NAOner R et al., 2000Oner R, Gümrük F, Acar C, Oner C, Gürgey A, Altay C, . Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.. Haematologica. 2000; 85(3):320-1

References

Daoud BB, Mosbehi I, Préhu C, Chaouachi D, Hafsia R, Abbes S, Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia.Pathol. Biol.. 2008; 56(5):260-7

Martinez di Montemuros F, Dotti C, Tavazzi D, Fiorelli G, Cappellini MD, Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy.Haematologica. 1997; 82(4):440-5

Oner R, Gümrük F, Acar C, Oner C, Gürgey A, Altay C, Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.Haematologica. 2000; 85(3):320-1