Nepal Journal of Neuroscience (May 2018)

Joubert Syndrome: A Case Report

  • Prakash Kafle ,
  • Sushil Krishna Shilpakar,
  • Mohan Raj Sharma,
  • Gopal Sedain,
  • Amit K Pradhanang,
  • Binod Raj Bhandari

DOI
https://doi.org/10.3126/njn.v15i1.20023
Journal volume & issue
Vol. 15, no. 1
pp. 33 – 36

Abstract

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Joubert syndrome (JS) isa rare autosomal recessive neuro developmental disorder involving cerebellar vermis and brainstem, marked by agenesis of cerebellar vermis, ataxia, hypotonia, oculomotor apraxia, neonatal breathing problems and mental retardation. Magnetic Resonance Imaging (MRI) reveals the characteristic Molar tooth sign of midbrain and Batwing appearance of rostral fourth ventricle.

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