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dyssynergia mozočka myoklonická
Record number d002527 Date 06.06.2025 Type M - MESH Topical term dyssynergia mozočka myoklonická Other term English (Pseudonym) Cerebellar Dyssynergia
English (Pseudonym) Dentate Cerebellar Atrophy
English (Pseudonym) Dyssynergia Cerebellaris Myoclonica
English (Pseudonym) Ramsay Hunt Cerebellar Syndrome
Slovak (Pseudonym) dyssynergia mozočka
Slovak (Pseudonym) atrofia ozubeného jadra mozočka
Slovak (Pseudonym) nucleus dentatus, atrofia
Slovak (Pseudonym) dyssynergia cerebellaris myoclonica
Slovak (Pseudonym) Ramsay Huntov mozočkový syndróm
UDC C10.228.140.252.700.250C10.228.854.787.500C10.574.500.825.250C16.320.400.780.500 Note A condition marked by progressive CEREBELLAR ATAXIA combined with MYOCLONUS usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal SEIZURES, spasticity, and DYSKINESIAS. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the CEREBELLUM are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. (From Joynt, Clinical Neurology, 1991, Ch37, pp60-1) 
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Number of the records: 1