Autonomic dysfunction in a patient with X-linked adrenoleukodystrophy

Int J Neurosci. 2018 Aug;128(8):783-784. doi: 10.1080/00207454.2017.1405953. Epub 2017 Dec 28.

Abstract

X-linked adrenoleukodystrophy is an inherited disease caused by abnormal accumulation of very long chain fatty acids. The diagnosis of X-linked adrenoleukodystrophy can be confirmed with the mutation of ABCD1 gene. The main symptom of the X-linked adrenoleukodystrophy is spastic paraparesis, and autonomic dysfunction is rare in X-linked adrenoleukodystrophy. Here, we presented an X-ALD case of a 46-year-old Asian male with severe autonomic dysfunction. Impairment of the autonomic nervous system may closely relate to mitochondrial defect.

Keywords: X-linked adrenoleukodystrophy; autonomic dysfunction; mitochondrial defect.

Publication types

  • Case Reports

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily D, Member 1 / genetics
  • Adrenoleukodystrophy / complications*
  • Autonomic Nervous System Diseases / etiology*
  • Humans
  • Middle Aged
  • Mutation / genetics
  • Severity of Illness Index

Substances

  • ATP Binding Cassette Transporter, Subfamily D, Member 1