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Joubert syndrome with autism in two siblings: A rare presentation
Joubert syndrome is a rare autosomal recessive disorder with partial or complete agenesis of cerebellar vermis. This syndrome is identified mainly by the presence of molar tooth sign in magnetic resonance imaging of the brain since it has a varied phenotypic presentation. Of the 200 cases reported s...
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| Foilsithe in: | Indian J Psychiatry |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Medknow Publications & Media Pvt Ltd
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4776590/ https://ncbi.nlm.nih.gov/pubmed/26985112 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5545.174395 |
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