Abstract
Joubert syndrome is a rare neurological disorder. It is characterized by the absence or underdevelopment of the cerebellar vermis and a malformed brain stem. These abnormalities cause signs and symptoms that include abnormal breathing patterns, hypotonia and development delay. It may associate kidney, liver or eye abnormalities. Treatment is supportive and depends on the symptoms in each person. This is why early diagnosis is so important, to offer a multidisciplinary strategy for improving the prognosis and quality of life.
Author supplied keywords
Cite
CITATION STYLE
Cintora, S. M., Suárez, A. S., Álvarez, M. H., Aguado, I. C., Pascual, E. A., Lobato, E. S., & Benítez, E. M. (2021). Joubert syndrome. Pediatria de Atencion Primaria, 23(90), 191–194. https://doi.org/10.37549/jpcr-25-0037
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.