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Chronic vomiting revealing Joubert syndrome: A case report
Leila Haddar1, Asmae Kasimi1, Karim Haddar1
1Department of Radiology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed First, Oujda, Morocco.
Insights
Joubert syndrome, a rare genetic disorder, is identified by the distinctive "molar tooth" sign on brain imaging. This case highlights its varied presentation, including chronic vomiting, in a young patient.
Area of Science:
- Neurology
- Radiology
- Genetics
Background:
- Joubert syndrome is a rare autosomal recessive ciliopathy.
- It is characterized by a distinctive "molar tooth" sign on neuroimaging.
- Clinical presentation can be variable, potentially leading to diagnostic challenges.
Abstract:
Joubert syndrome is a rare autosomal recessive disorder characterized by the presence of the molar tooth sign on imaging. We report the case of a 5-year-old girl diagnosed with Joubert syndrome during the investigation of chronic vomiting. The patient presented with neuropsychomotor delay, a history of neonatal respiratory disorders, and hydrocephalus treated with a ventriculoperitoneal shunt. Brain magnetic resonance imaging revealed a deepened interpeduncular fossa, thickening and horizontalization of the upper cerebellar peduncles, and vermian hypoplasia, resulting in the characteristic "molar tooth" appearance. The neuropsychomotor delay was attributed to Joubert syndrome, while the chronic vomiting was linked to hyperdrainage. This case underscores the potential for clinical signs of Joubert syndrome to confuse clinicians and highlights the importance of recognizing the pathognomonic molar tooth sign in imaging, which all radiologists should be familiar with.
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