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Joubert syndrome: Clinical and radiological characteristics of nine patients
BACKGROUND: Joubert Syndrome (JS) is a rare genetic developmental disorder, first identified in 1969. In patients with JS, certain regions of the brain (mainly cerebellar vermis and brainstem) are underdeveloped or malformed. This can lead to impaired attention, visual, spatial, motor, language and...
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| Main Authors: | , |
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| Format: | Artigo |
| Language: | Inglês |
| Published: |
Medknow Publications & Media Pvt Ltd
2013
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3724083/ https://ncbi.nlm.nih.gov/pubmed/23956573 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0972-2327.112480 |
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