Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism

Hum Mutat. 1999;14(6):477-84. doi: 10.1002/(SICI)1098-1004(199912)14:6<477::AID-HUMU6>3.0.CO;2-X.

Abstract

DNA sequencing revealed seven different glucose-6-phosphate dehydrogenase (G6PD) mutations in G6PD deficient subjects from 10 Polish families. Among them we found two novel mutations: 679C-->T (G6PD Radlowo, class 2) and a 1006A-->G (G6PD Torun, class 1). Variant G6PD Radlowo was characterized biochemically. Both novel mutations were analyzed using a model of the tertiary structure of the human enzyme. The main chain of G6PD Torun is different from the wild-type G6PD. The remaining mutations identified by us in deficient Polish patients were: 542A-->T (G6PD Malaga), 1160G-->A (G6PD Beverly Hills), 1178G-->A (G6PD Nashville), 1192G-->A (G6PD Puerto Limon), and 1246G-->A (G6PD Tokyo). Variant Tokyo was found in four families. In one of them favism was the first clinical sign of G6PD deficiency and chronic nonspherocytic hemolytic anemia (CNSHA) was diagnosed later. Variants G6PD Nashville and G6PD Puerto Limon were accompanied by the silent mutation 1311C-->T of the G6PD gene.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Anemia, Hemolytic, Congenital Nonspherocytic / enzymology*
  • Anemia, Hemolytic, Congenital Nonspherocytic / genetics*
  • Base Sequence
  • Child
  • Child, Preschool
  • Chronic Disease
  • DNA Primers / genetics
  • Favism / enzymology*
  • Favism / genetics*
  • Female
  • Genetic Variation
  • Glucosephosphate Dehydrogenase / chemistry
  • Glucosephosphate Dehydrogenase / genetics*
  • Glucosephosphate Dehydrogenase Deficiency / enzymology*
  • Glucosephosphate Dehydrogenase Deficiency / genetics*
  • Humans
  • Male
  • Middle Aged
  • Models, Molecular
  • Pedigree
  • Phenotype
  • Point Mutation*
  • Poland
  • Protein Conformation

Substances

  • DNA Primers
  • Glucosephosphate Dehydrogenase