Adenylosuccinase deficiency: an unusual cause of early-onset epilepsy associated with acquired microcephaly

Brain Dev. 2000 Sep;22(6):383-6. doi: 10.1016/s0387-7604(00)00154-6.

Abstract

Adenylosuccinase deficiency, an autosomal recessive inborn error of purine synthesis, was first described in 1984 by Jaeken and Van den Berghe (reviewed in J Inher Metab Dis 20;1997:193). The cardinal features are variable psychomotor delay often accompanied by epilepsy and autistic features. Diagnosis is made by detection of abnormal purine metabolites in body fluids. We report a girl who presented with early onset epilepsy, associated with acquired microcephaly and severe psychomotor retardation, as the most prominent symptoms.

Publication types

  • Case Reports

MeSH terms

  • Adenylosuccinate Lyase / deficiency*
  • Age of Onset
  • Brain / metabolism
  • Brain / pathology
  • Brain / physiopathology
  • Brain Diseases, Metabolic, Inborn / complications*
  • Brain Diseases, Metabolic, Inborn / diagnosis
  • Brain Diseases, Metabolic, Inborn / pathology
  • Child, Preschool
  • Disease Progression
  • Electroencephalography
  • Epilepsy / etiology*
  • Epilepsy / metabolism*
  • Epilepsy / pathology
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Microcephaly / etiology*
  • Microcephaly / metabolism*
  • Microcephaly / pathology

Substances

  • Adenylosuccinate Lyase