Mutational analysis of carbamoylphosphate synthetase I deficiency in three Japanese patients

J Inherit Metab Dis. 2004;27(6):787-8. doi: 10.1023/b:boli.0000045842.59768.ea.

Abstract

We describe the results of mutational analysis of the carbamoylphosphate synthetase I (CPSI) gene in three nonconsanguineous patients with CPSI deficiency. Compound heterozygotes of 3422T/G (V1141G) plus 3784C/T (R1262X), 1528delG (510-514 ARQLX) plus 2752T/C (S918P), and 2549G/A (R850H) plus 2797delT (L933X) were identified through genomic analysis; however, the 2797delT (L933X) mutation was not detected in cDNA analysis using biopsied liver, suggesting that mRNA expression rom this mutant allele is absent or markedly low.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Carbamoyl-Phosphate Synthase (Ammonia) / genetics*
  • Carbamoyl-Phosphate Synthase I Deficiency Disease / genetics*
  • DNA Mutational Analysis
  • DNA, Complementary / genetics
  • Female
  • Heterozygote
  • Humans
  • Infant, Newborn
  • Japan
  • Liver / metabolism
  • Liver / pathology
  • Male
  • RNA, Messenger / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • DNA, Complementary
  • RNA, Messenger
  • Carbamoyl-Phosphate Synthase (Ammonia)