Misdiagnosis of multiple sclerosis in a female heterozygote with Fabry's disease

Mult Scler Relat Disord. 2019 May:30:45-47. doi: 10.1016/j.msard.2019.01.040. Epub 2019 Jan 30.

Abstract

Fabry's disease is an X-linked disorder of enzyme alpha-galactosidase A which leads to an accumulation of the glycolipids in lysosomes in vessels and organs. The disorder is rare with an estimated incidence of 1 in 40,000 and disease occurs more rarely in women than men. Paresthesias, hearing loss, and stroke are the typical neurological manifestations. Brain magnetic resonance imaging abnormalities may mimic those seen in multiple sclerosis (MS). Reported here is one of the rarely reported cases of Fabry's disease in a female heterozygote mistaken for MS.

Keywords: Fabry's disease; Magnetic resonance imaging; Multiple sclerosis; Paresthesia.

Publication types

  • Case Reports

MeSH terms

  • Diagnosis, Differential
  • Diagnostic Errors
  • Fabry Disease / diagnosis*
  • Fabry Disease / genetics
  • Female
  • Heterozygote
  • Humans
  • Middle Aged
  • Multiple Sclerosis / diagnosis*
  • Rare Diseases