Joubert Syndrome: A Rare Radiological Case

Joubert syndrome is a rare autosomal recessive neurodevelopmental disease characterized by abnormal breathing patterns composed of episodic tachypnea/apnea, hypotonia, ataxia, developmental delay, intellectual impairment, ocular impairment, renal cysts, and hepatic fibrosis. We report the case of a...

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Detalles Bibliográficos
Autores principales: Akhtar, Ali, Hassan, Syed Adeel, Falah, Noor Ul, Khan, Maham, Sheikh, Fahad N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Radiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970099/
https://www.ncbi.nlm.nih.gov/pubmed/31988813
http://dx.doi.org/10.7759/cureus.6410

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970099/
https://www.ncbi.nlm.nih.gov/pubmed/31988813
http://dx.doi.org/10.7759/cureus.6410

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