Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritance

Brain Dev. 1998 Mar;20(2):116-8. doi: 10.1016/s0387-7604(97)00109-5.

Abstract

Paroxysmal tonic upgaze of childhood with ataxia is a rare form of age related dystonia. Out of 12 previously reported cases, three had a clinical history of similar symptoms occurring in at least one first degree relative belonging to the same or two consecutive generations. Autosomal dominant inheritance was therefore hypothesized. We report on a family in which the disorder appeared in three consecutive generations between ages 6 and 11 months, disappearing gradually and spontaneously between ages 18 to 24 months. All affected individuals had normal neurologic development. The pedigree analysis of previously reported cases and of the family reported herein provides strong evidence that the disorder may be inherited as an autosomal dominant trait and represents a form of transient paroxysmal dystonia with benign long-term prognosis.

Publication types

  • Case Reports

MeSH terms

  • Ataxia / genetics
  • Ataxia / physiopathology*
  • Child, Preschool
  • Dystonia / genetics
  • Dystonia / physiopathology*
  • Female
  • Fixation, Ocular / genetics
  • Fixation, Ocular / physiology*
  • Humans
  • Male
  • Ocular Motility Disorders / genetics
  • Ocular Motility Disorders / physiopathology*
  • Pedigree