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CASE REPORT
Year : 2016  |  Volume : 2  |  Issue : 1  |  Page : 51-53

Joubert syndrome misdiagnosed as hypotonic cerebral palsy: Confirmation by magnetic resonance imaging


Department of Radiodiagnosis and Imaging, Government Medical College, Jammu and Kashmir, India

Correspondence Address:
Mohd Ilyas
Lane 22, House No. 38, Tawi Vihar, Sidhra,Jammu 180 019, Jammu and Kashmir
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2395-4264.188165

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Joubert syndrome is a rare autosomal recessive condition characterized by hypotonia, ataxia, psychomotor delay, and variable occurrence of oculomotor apraxia and neonatal breathing abnormalities. We report a 7-year-old female child who was referred to our department as a case developmental delay and hypotonia due to hypotonic cerebral palsy for magnetic resonance imaging (MRI) of the brain. MRI of the brain revealed typical molar tooth sign, bat wing appearance of the fourth ventricle, and dysgenesis of the superior cerebellar vermis. Determination of the symptoms, early diagnosis, and genetic consultation are the goals for decision-making to begin treatment and rehabilitation programs.


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