FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9

Ann Clin Transl Neurol. 2020 Apr;7(4):565-572. doi: 10.1002/acn3.51005. Epub 2020 Mar 12.

Abstract

We report four patients from two families who presented attacks of childhood-onset episodic ataxia associated with pathogenic mutations in the FGF14 gene. Attacks were triggered by fever, lasted several days, and had variable frequencies. Nystagmus and/or postural tremor and/or learning disabilities were noticed in individuals harboring FGF14 mutation with or without episodic ataxia. These cases and literature data delineate the FGF14-mutation-related episodic ataxia phenotype: wide range of age at onset (from childhood to adulthood), variable durations and frequencies, triggering factors including fever, and association to chronic symptoms. We propose to add FGF14-related episodic ataxia to the list of primary episodic ataxia as Episodic Ataxia type 9.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Ataxia / genetics*
  • Ataxia / physiopathology*
  • Child
  • Child, Preschool
  • Female
  • Fibroblast Growth Factors / genetics*
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Phenotype

Substances

  • fibroblast growth factor 14
  • Fibroblast Growth Factors

Supplementary concepts

  • Episodic Ataxia

Grants and funding

This work was funded by Clinical Research Hospital Program from the French Ministry of Health grant 14‐12.