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Joubert Syndrome: A Molar Tooth Sign in Disguise
Joubert syndrome (JS) is a rare genetic ciliopathy characterized by the aplasia or malformation of the midbrain and or hindbrain structures. It usually manifests during the early stages with nonspecific neurological symptoms that progress to involve multiple systems. Its presentation similarity to o...
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| Publié dans: | Cureus |
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| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Cureus
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7489322/ https://ncbi.nlm.nih.gov/pubmed/32944439 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.9718 |
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