[Genetic counseling in ornithine carbamoyltransferase deficiency]

Ann Biol Clin (Paris). 1988;46(7):455-9.
[Article in French]

Abstract

Ornithine transcarbamylase (OTC) deficiency is an inborn error of urea cycle metabolism, responsible for lethal hyperammonemia in males and for severe symptoms in at least 20% of heterozygous females. The authors provide here additional data on the informativity of the protein loading test (PLT) for the detection of heterozygotes. They show that the risk of being a carrier for the mother of an affected boy falls from 2/3 a priori to only 1/8 if her PLT is negative. The risk for the mother of heterozygote girl falls from 1/2 a priori to 1/16 if her PLT is negative.

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / genetics*
  • Ammonia / blood*
  • Chromosome Mapping
  • Female
  • Genetic Carrier Screening / methods*
  • Genetic Counseling*
  • Genetic Linkage
  • Humans
  • Male
  • Ornithine Carbamoyltransferase / genetics
  • Ornithine Carbamoyltransferase Deficiency Disease*
  • Orotic Acid / urine
  • Pedigree
  • Polymorphism, Restriction Fragment Length
  • Risk Factors

Substances

  • Orotic Acid
  • Ammonia
  • Ornithine Carbamoyltransferase