Climber exhibits first clinical manifestation of spinocerebellar ataxia on Karakoram expedition

J Travel Med. 2022 Aug 20;29(5):taac020. doi: 10.1093/jtm/taac020.

Abstract

Spinocerebellar ataxias are rare, genetically inherited diseases. Their typical symptoms include disturbances in gait, balance and uncoordinated movements, but these abnormalities, when appear at altitude, might also suggest high-altitude cerebral edema.

We described the first clinical manifestation of spinocerebellar ataxia of a climber from Poland on a Karakoram expedition.

Keywords: Spinocerebellar ataxia; high altitude; inherited disease; neurodegeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Expeditions*
  • Humans
  • Spinocerebellar Ataxias* / diagnosis