Cerebellar cognitive affective syndrome: insights from Joubert syndrome

Abstract Background Joubert syndrome (JS) is a rare, autosomal recessively inherited genetic disorder characterized morphologically by unique developmental malformations of the cerebellum and brainstem (the molar tooth sign), and clinically by impaired motor functions and intellectual disability. Pa...

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Bibliographic Details
Main Authors: Chelsea L. Hickey, Janet C. Sherman, Paula Goldenberg, Amy Kritzer, Paul Caruso, Jeremy D. Schmahmann, Mary K. Colvin
Format: Article
Language:English
Published: BMC 2018-03-01
Series:Cerebellum & Ataxias
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40673-018-0085-y