CEREBELLAR SYNDROME
نویسندگان
چکیده
منابع مشابه
[Cerebellar cognitive affective syndrome].
INTRODUCTION The diagnosis of Cerebellar Cognitive Affective Syndrome should be considered in patients with cerebellar lesions who also suffer cognitive deficits associated with visuospatial or executive neuropsychological disorders, expressive language disorders and affective disorders. CLINICAL CASE A 16 year old adolescent diagnosed with Attention Deficit Hyperactivity Disorder at the age ...
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A 63 year old woman who presented with a cerebellar syndrome was shown to have sarcoidosis of the central nervous system, skin and liver with no pulmonary involvement.
متن کاملThe cerebellar cognitive affective syndrome.
Anatomical, physiological and functional neuroimaging studies suggest that the cerebellum participates in the organization of higher order function, but there are very few descriptions of clinically relevant cases that address this possibility. We performed neurological examinations, bedside mental state tests, neuropsychological studies and anatomical neuroimaging on 20 patients with diseases ...
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A 64-year-old man presented with sudden onset of right-sided hemiparesis, headache, gait disturbance, and recurrent vomiting. A physical examination revealed right-sided hemiparesis, right Horner syndrome, ataxia of the right limbs, and diminished sensation on the left side of his body. Diffusion-weighted MRI revealed an acute right lateral medullary infarction extending from the rostral medull...
متن کاملCerebellar cognitive affective syndrome: insights from Joubert syndrome
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. Patients with JS often face multiple cognitive challenges, but the neuropsychological profile of this condit...
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ژورنال
عنوان ژورنال: The Journal of Nervous and Mental Disease
سال: 1915
ISSN: 0022-3018
DOI: 10.1097/00005053-191505000-00002