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dyssynergia mozočka myoklonická
Č. záznamu d002527 Dátum 06.06.2025 Typ M - MESH Tematický termín dyssynergia mozočka myoklonická Iný termín Angličtina (Pseudonym) Cerebellar Dyssynergia
Angličtina (Pseudonym) Dentate Cerebellar Atrophy
Angličtina (Pseudonym) Dyssynergia Cerebellaris Myoclonica
Angličtina (Pseudonym) Ramsay Hunt Cerebellar Syndrome
Slovenčina (Pseudonym) dyssynergia mozočka
Slovenčina (Pseudonym) atrofia ozubeného jadra mozočka
Slovenčina (Pseudonym) nucleus dentatus, atrofia
Slovenčina (Pseudonym) dyssynergia cerebellaris myoclonica
Slovenčina (Pseudonym) Ramsay Huntov mozočkový syndróm
MDT C10.228.140.252.700.250C10.228.854.787.500C10.574.500.825.250C16.320.400.780.500 Poznámka 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) predmetové heslo
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