Neuropediatrics 1995; 26(6): 322-324
DOI: 10.1055/s-2007-979783
Short communications

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A Mild Form of Infantile Isolated Sulphite Oxidase Deficiency

C. Barbot1 , E. Martins1 , L. Vilarinho2 , C. Dorche3 , M. L. Cardoso2
  • 1Serviço de Neuropediatria, Hospital de Crianças Maria Pia, Porto, Portugal
  • 2Instituto de Genética Médica Jacinto de Magalhães, Porto, Portugal
  • 3Service de Biochimie, Hôpital Debrousse, Lyon, France
Further Information

Publication History

Publication Date:
19 April 2007 (online)

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Abstract

Neonatal sulphite oxidase deficiency is characterised by severe neurologic dysfunction, brain atrophy, dislocation of the lens and increased urinary excretion of sulphite, thiosulphate, taurine and S-sulphocysteine, and by a low plasma cystine. We present clinical, neuroradiological and biochemical data of a patient with late onset symptoms comparing this presentation with the neonatal form and stressing the difficulties of the diagnosis of this disorder.