Pyrimidine 5'-nucleotidase deficiency: improved detection of carriers

Clin Chim Acta. 1989 Sep 29;184(2):175-80. doi: 10.1016/0009-8981(89)90287-8.

Abstract

The activities of pyrimidine 5'-nucleotidase (P5N) and the nucleotide pools in the erythrocytes from 19 members of a Dutch family with P5N deficiency were measured. In the erythrocytes of 5 (out of 6) apparent heterozygotes (based on P5N activities), an increased amount of UDP-N-acetylhexosamines was found. This increase was also found in the erythrocytes of 2 (out of 3) questionable heterozygotes (P5N activity below normal range, but not below normal mean--2 X SD) and not in the erythrocytes of family members with a normal P5N activity nor in erythrocytes from healthy donors. We conclude that analysis of the ribonucleotide patterns, in combination with determination of P5N activity, allows a more accurate diagnosis of heterozygosity for P5N.

Publication types

  • Case Reports

MeSH terms

  • 5'-Nucleotidase / deficiency*
  • 5'-Nucleotidase / genetics
  • Anemia, Hemolytic, Congenital / enzymology*
  • Anemia, Hemolytic, Congenital Nonspherocytic / enzymology*
  • Anemia, Hemolytic, Congenital Nonspherocytic / genetics
  • Erythrocytes / analysis
  • Erythrocytes / enzymology*
  • Female
  • Genetic Carrier Screening / methods*
  • Humans
  • Infant, Newborn
  • Nucleotides / analysis
  • Nucleotides / genetics
  • Uridine Diphosphate N-Acetylgalactosamine / analysis
  • Uridine Diphosphate N-Acetylglucosamine / analysis

Substances

  • Nucleotides
  • Uridine Diphosphate N-Acetylglucosamine
  • Uridine Diphosphate N-Acetylgalactosamine
  • 5'-Nucleotidase