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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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| Publicat a: | Cureus |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Cureus
2020
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| Matèries: | |
| Accés en línia: | 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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