A Novel Point Mutation in X-linked Adrenoleukodystrophy Presenting as a Spinocerebellar Degeneration

Ann Neurol. 1999 May;45(5):652-5. doi: 10.1002/1531-8249(199905)45:5<652::aid-ana14>3.0.co;2-m.

Abstract

X-linked adrenoleukodystrophy (ALD) usually presents in childhood as severe cerebral demyelination accompanied by axonal loss or in adults as a progressive spinal cord syndrome (adrenomyeloneuropathy). Rarely, patients present with adult onset spinocerebellar ataxia. We performed mutation analysis in a family with several members who had this rare phenotype and identified a single nucleotide deletion in exon 2 of the ALD gene. This is the first mutation analysis to be reported in this unusual phenotypic variant of ALD and the first deletion to be reported in exon 2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenoleukodystrophy / genetics*
  • Genetic Linkage / genetics
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Phenotype
  • Point Mutation / genetics*
  • Spinocerebellar Degenerations / genetics*
  • X Chromosome / genetics*