Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 88-93 |
| Number of pages | 6 |
| Journal | Journal of Krishna Institute of Medical Sciences University |
| Volume | 10 |
| Issue number | 3 |
| Publication status | Published - 2021 |
All Science Journal Classification (ASJC) codes
- General Medicine
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