Macrocerebellum in Achondroplasia: A Further CNS Manifestation of FGFR3 Mutations?

AJNR Am J Neuroradiol. 2020 Feb;41(2):338-342. doi: 10.3174/ajnr.A6369. Epub 2019 Dec 19.

Abstract

Achondroplasia is the result of a mutation in the fibroblast growth factor receptor 3 gene (FGFR3). Appearances suggestive of macrocerebellum have not been described in this patient group. We retrospectively reviewed MR imaging studies of the brain in 23 children with achondroplasia. A constellation of imaging findings that are recognized in macrocerebellum was observed, including cerebellar hemisphere enlargement (inferior and superior extension, wrapping around the brainstem); an effaced retro- and infravermian cerebellar subarachnoid CSF space; a shortened midbrain; distortion of the tectal plate; and mass effect on the brainstem. All MR imaging studies exhibited some of these findings. Quantitative analysis confirmed an increased cerebellar volume compared with age- and sex-matched controls. We hypothesized that this may be due to direct effects of the FGFR3 mutation on cerebellar morphogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Achondroplasia / genetics*
  • Achondroplasia / pathology*
  • Cerebellum / pathology*
  • Child
  • Female
  • Humans
  • Magnetic Resonance Imaging / methods
  • Male
  • Mutation
  • Organ Size
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics*
  • Retrospective Studies

Substances

  • FGFR3 protein, human
  • Receptor, Fibroblast Growth Factor, Type 3