Joubert Syndrome (JS) is a rare congenital condition first reported by French Neurologist Marie Joubert in 1969 which shows multi-organ manifestations including developmental, neurological, renal, hepatic, ocular and orofacial abnormalities. This condition also shows a unique neuro-radiological imaging feature “Molar Tooth Sign” (MTS) in MRI. We report a case of a young boy of consanguineous parents who presented to the dental department with some unique orofacial features along with a discussion on the various general, orofacial, and imaging features and management of this condition.
|Number of pages||6|
|Journal||Journal of Krishna Institute of Medical Sciences University|
|Publication status||Published - 2021|
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