Search on: MYOCLONIC CEREBELLAR DYSSYNERGIA 
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Descriptor English:   Myoclonic Cerebellar Dyssynergia 
Descriptor Spanish:   disinergia cerebelosa mioclónica 
Descriptor Portuguese:   Dissinergia Cerebelar Mioclônica 
Synonyms English:   Ataxia, Dentate Cerebellar
Ataxias, Dentate Cerebellar
Atrophies, Dentate Cerebellar
Atrophy, Dentate Cerebellar
Cerebellar Ataxias, Dentate
Cerebellar Atrophy, Dentate
Cerebellar Dyssynergia
Cerebellar Dyssynergia, Myoclonic
Cerebellar Dyssynergias
Cerebellar Dyssynergias, Myoclonic
Cerebelloparenchymal Disorder V
Dentate Cerebellar Ataxia
Dentate Cerebellar Ataxias
Dentate Cerebellar Atrophies
Dentate Cerebellar Atrophy
Dentate Nucleus Syndrome, Ramsay Hunt
Dyssynergia Cerebellaris Myoclonica
Dyssynergia Cerebellaris Myoclonica Of Hunt
Dyssynergia Cerebellaris Progressiva
Dyssynergia, Cerebellar
Dyssynergia, Myoclonic Cerebellar
Dyssynergias, Cerebellar
Dyssynergias, Myoclonic Cerebellar
Myoclonic Cerebellar Dyssynergias
Ramsay Hunt Cerebellar Syndrome
Ramsay Hunt Dentate Syndrome
Spinodentate Atrophy  
Tree Number:   C10.228.140.252.700.250
C10.228.854.787.500
C10.574.500.825.250
C16.320.400.780.500
Definition English:   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) 
Indexing Annotation English:   do not confuse X ref RAMSAY HUNT CEREBELLAR SYNDROME with RAMSAY HUNT AURICULAR SYNDROME see HERPES ZOSTER OTICUS or RAMSAY HUNT PARALYSIS SYNDROME see PARKINSONIAN DISORDERS
History Note English:   2000(1970); use CEREBELLAR ATAXIA 1970-1990 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DG diagnostic imaging
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RT radiotherapy RH rehabilitation
SU surgery TH therapy
UR urine VE veterinary
VI virology  
Record Number:   22381 
Unique Identifier:   D002527 

Occurrence in VHL: 		 

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