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Joubert syndrome
Joubert syndrome (JS) is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones
Pronunciation
/ˈjaʊbərt ˈsɪnˌdroʊm/
Categories
autosomal recessive
ciliopathy
encephalopathy
rare disease