Idiopathic central pontine myelinolysis in childhood

Dev Med Child Neurol. 2001 Oct;43(10):697-700. doi: 10.1017/s0012162201001256.

Abstract

Central pontine myelinolysis (CPM) is rare in childhood with only a few cases reported in world literature. We report a 7-year-old male who presented with acute ataxia, swallowing difficulties, dysarthria, and radiological features consistent with the disorder. He improved remarkably with oral prednisolone therapy and was almost back to normal by 2 weeks. A review of the literature is also included.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Anti-Inflammatory Agents / therapeutic use
  • Child
  • Humans
  • Male
  • Myelinolysis, Central Pontine / drug therapy
  • Myelinolysis, Central Pontine / pathology*
  • Myelinolysis, Central Pontine / physiopathology*
  • Pons / pathology
  • Pons / physiopathology
  • Prednisolone / therapeutic use

Substances

  • Anti-Inflammatory Agents
  • Prednisolone