Journal of Inherited Metabolic Disease

, Volume 24, Issue 3, pp 370–378

Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry

Authors

  • S. Stadler
    • Institut für Klinische ChemieMolekulare Diagnostik und Mitochondriale Genetik
  • K. Gempel
    • Institut für Klinische ChemieMolekulare Diagnostik und Mitochondriale Genetik
  • I. Bieger
    • Institut für Klinische ChemieMolekulare Diagnostik und Mitochondriale Genetik
  • B. F. Pontz
    • Kinderklinik der Technischen Universität München
  • K.-D. Gerbitz
    • Institut für Klinische ChemieMolekulare Diagnostik und Mitochondriale Genetik
  • M. F. Bauer
    • Institut für Klinische ChemieMolekulare Diagnostik und Mitochondriale Genetik
  • S. Hofmann
    • Institut für Klinische ChemieMolekulare Diagnostik und Mitochondriale Genetik
Article

DOI: 10.1023/A:1010560704092

Cite this article as:
Stadler, S., Gempel, K., Bieger, I. et al. J Inherit Metab Dis (2001) 24: 370. doi:10.1023/A:1010560704092

Abstract

Argininosuccinate lyase (ASL) deficiency (McKusick 207900) is an inborn error of the urea cycle. The leading symptom is progressive hyperammonaemia, which is a life-threatening condition, particularly in patients with a neonatal onset. Early diagnosis and treatment of the hyperammonaemia are necessary to improve survival and the long-term outcome of ASL-deficient patients. Currently, the diagnosis of ASL deficiency is based on the measurement of urea cycle intermediates and amino acids by automated quantitative ion exchange chromatography in plasma and urine. Here, we report a newborn presenting with coma and severe hyperammonaemia. ASL deficiency was suspected on the basis of an adapted tandem mass spectrometric (MS-MS) procedure which allows determination of argininosuccinate in addition to the amino acids in serum samples. MS-MS measurements revealed a characteristic increase of argininosuccinate, a moderate increase of citrulline, and lowered levels of arginine and ornithine in the serum of the patient. The diagnosis was confirmed by the detection of a novel homozygous frameshift mutation in exon 14 of the argininosuccinate lyase gene. We propose MS-MS as a diagnostic tool suitable for the rapid detection of specific alterations in the amino acid spectra caused by ASL deficiency.

Copyright information

© Kluwer Academic Publishers 2001