Biomaterial Database

[Hereditary spino-cerebellar degeneration and Ramsay-Hunt disease]. 1974

D Penneau, and J C Bigorgne, and L Fressinaud-Masdefeix

UI	MeSH Term	Description	Entries
D008297	Male		Males
D002524	Cerebellar Ataxia	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)	Adiadochokinesis,Ataxia, Cerebellar,Cerebellar Dysmetria,Dysmetria,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
D002526	Cerebellar Diseases	Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA.	Cerebellar Dysfunction,Cerebellum 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
D002527	Myoclonic Cerebellar Dyssynergia	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)	Cerebellar Dyssynergia,Dentate Cerebellar Atrophy,Dyssynergia Cerebellaris Myoclonica,Ramsay Hunt Cerebellar Syndrome,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
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328	Adult	A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available.	Adults
D013118	Spinal Cord Diseases	Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord.	Myelopathy,Spinal Cord Disorders,Myelopathies,Spinal Cord Disease,Spinal Cord Disorder