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 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.252 Cerebellar Diseases .
C10.228.140.252.190 Cerebellar Ataxia .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.140.252.700.250 Myoclonic Cerebellar Dyssynergia .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.228.854.787.500 Myoclonic Cerebellar Dyssynergia .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.825 Spinocerebellar Degenerations .
C10.574.500.825.250 Myoclonic Cerebellar Dyssynergia .
C10.597 Neurologic Manifestations .
C10.597.350 Dyskinesias .
C10.597.350.090 Ataxia .
C10.597.350.090.500 Cerebellar Ataxia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.780 Spinocerebellar Degenerations .
C16.320.400.780.500 Myoclonic Cerebellar Dyssynergia .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.350 Dyskinesias .
C23.888.592.350.090 Ataxia .
C23.888.592.350.090.200 Cerebellar Ataxia .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Cerebellar Diseases .
Cerebellar Disorders .
Cerebellar Syndromes .
Cerebellar Disease .
Cerebellar Disorder .
Cerebellar Dysfunctions .
Cerebellar Syndrome .
Cerebellum Disease .
Disease, Cerebellar .
Disease, Cerebellum .
Disorder, Cerebellar .
Dysfunction, Cerebellar .
Syndrome, Cerebellar .
Cerebellar Dysfunction .
Cerebellum Diseases .
Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. .
1.00
975551
 
/physiopathology .
/dysfunction .
/pathophysiology .
/functional pathology .
/pathologic physiology .
Used with organs and diseases for disordered function in disease states. .
0.70
 
Cerebellar Ataxia .
Cerebellar Hemiataxia .
Cerebellar Incoordination .
Hypermetria .
Adiadochokineses .
Ataxias, Cerebellar .
Cerebellar Ataxias .
Cerebellar Dysmetrias .
Cerebellar Hemiataxias .
Cerebellar Incoordinations .
Dysmetria, Cerebellar .
Dysmetrias .
Dysmetrias, Cerebellar .
Hemiataxia, Cerebellar .
Hemiataxias, Cerebellar .
Hypermetrias .
Incoordination, Cerebellar .
Incoordinations, Cerebellar .
Ataxia, Cerebellar .
Adiadochokinesis .
Cerebellar Dysmetria .
Dysmetria .
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90) .
0.69
563869
 
Myoclonic Cerebellar Dyssynergia .
Cerebelloparenchymal Disorder V .
Dentate Cerebellar Ataxia .
Dentate Nucleus Syndrome, Ramsay Hunt .
Dyssynergia Cerebellaris Myoclonica Of Hunt .
Dyssynergia Cerebellaris Progressiva .
Ramsay Hunt Dentate Syndrome .
Spinodentate Atrophy .
Ataxia, Dentate Cerebellar .
Ataxias, Dentate Cerebellar .
Atrophies, Dentate Cerebellar .
Atrophy, Dentate Cerebellar .
Cerebellar Ataxias, Dentate .
Cerebellar Atrophy, Dentate .
Cerebellar Dyssynergia, Myoclonic .
Cerebellar Dyssynergias .
Cerebellar Dyssynergias, Myoclonic .
Dentate Cerebellar Ataxias .
Dentate Cerebellar Atrophies .
Dyssynergia, Cerebellar .
Dyssynergia, Myoclonic Cerebellar .
Dyssynergias, Cerebellar .
Dyssynergias, Myoclonic Cerebellar .
Myoclonic Cerebellar Dyssynergias .
Ramsay Hunt Cerebellar Syndrome .
Cerebellar Dyssynergia .
Dentate Cerebellar Atrophy .
Dyssynergia Cerebellaris Myoclonica .
RAMSAY HUNT DENTATE SYNDROME .
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) .
0.64
8174