Genetic and clinical studies on 19 families with adenine phosphoribosyltransferase deficiencies

Hum Genet. 1987 Feb;75(2):163-8. doi: 10.1007/BF00591080.

Abstract

Adenine phosphoribosyltransferase (APRT) deficiency leading to 2,8-dihydroxyadenine (DHA) urolithiasis has been considered a rare cause of urolithiasis and renal insufficiency. We have examined samples from 19 Japanese families with DHA lithiasis. In 79% of the families, patients only partially lacked hemolysate APRT activities, clearly contrasting with the complete deficiency in all the patients from non-Japanese families so far reported. All patients with DHA lithiasis were homozygotes for defective APRT genes, whether the deficiency was complete or partial. In family studies we found two symptomatic and four asymptomatic homozygous family members. The segregation figures are compatible with the hypothesis of a simple autosomal recessive mode of inheritance. By analyzing the data stored by a large clinical laboratory in Japan, we estimated that 0.00368% of the general population has DHA lithiasis. These data indicate that more than 1% of the general population possess mutant alleles of the APRT gene as heterozygotes. Our present studies indicate that most of the patients with this disease are undiagnosed in Japan, and probably in other countries also.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / analysis
  • Adenine Phosphoribosyltransferase / deficiency*
  • Adenine Phosphoribosyltransferase / genetics
  • Adolescent
  • Adult
  • Aged
  • Child, Preschool
  • Female
  • Gene Frequency
  • Heterozygote
  • Humans
  • Infant
  • Japan
  • Male
  • Middle Aged
  • Pentosyltransferases / deficiency*
  • Urinary Calculi / analysis
  • Urinary Calculi / enzymology
  • Urinary Calculi / genetics*

Substances

  • 2,8-dihydroxyadenine
  • Pentosyltransferases
  • Adenine Phosphoribosyltransferase
  • Adenine