Ataxia, hyperpnoea and mental retardation: was it the molar tooth?

BMJ Case Rep. 2010 Apr 29:2010:bcr10.2009.2331. doi: 10.1136/bcr.10.2009.2331.

Abstract

Joubert's syndrome is a rare autosomal recessive disease, which is under-diagnosed, associated with other brain and body malformations, and carries a poor prognosis. We describe a 6-year-old boy who presented with non-progressive instability of stance and gait, mental retardation and a new onset of generalised seizures with the typical brain imaging findings of Joubert's syndrome. We believe this is the first diagnosed case of Joubert's syndrome in Iraq.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple
  • Ataxia
  • Cerebellar Diseases / diagnosis*
  • Cerebellum / abnormalities
  • Child
  • Diagnosis, Differential
  • Eye Abnormalities / diagnosis*
  • Humans
  • Hyperventilation
  • Intellectual Disability
  • Iraq
  • Kidney Diseases, Cystic / diagnosis*
  • Magnetic Resonance Imaging
  • Male
  • Retina / abnormalities
  • Tomography, X-Ray Computed

Supplementary concepts

  • Agenesis of Cerebellar Vermis