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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.534 Muscular Disorders, Atrophic .
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 .
C10.228.140.252.190.530 Spinocerebellar Ataxias .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.140.252.700.250 Myoclonic Cerebellar Dyssynergia .
C10.228.140.252.700.700 Spinocerebellar Ataxias .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.228.854.787.500 Myoclonic Cerebellar Dyssynergia .
C10.228.854.787.875 Spinocerebellar Ataxias .
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 .
C10.574.500.825.700 Spinocerebellar Ataxias .
C10.597 Neurologic Manifestations .
C10.597.350 Dyskinesias .
C10.597.350.090 Ataxia .
C10.597.350.090.500 Cerebellar Ataxia .
C10.597.350.090.500.530 Spinocerebellar Ataxias .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
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 .
C16.320.400.780.875 Spinocerebellar Ataxias .
C23 Pathological Conditions, Signs and Symptoms .
C23.300 Pathological Conditions, Anatomical .
C23.300.070 Atrophy .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Muscular Disorders, Atrophic .
Atrophic Muscular Disorders .
Spinal and Bulbar Muscular Atrophy .
Spinobulbar Atrophy .
Spinopontine Atrophy .
Atrophic Muscular Disorder .
Atrophies, Disuse .
Atrophies, Spinobulbar .
Atrophies, Spinobulbar Muscular .
Atrophies, Spinopontine .
Atrophy, Spinobulbar .
Atrophy, Spinobulbar Muscular .
Disorder, Atrophic Muscular .
Disorders, Atrophic Muscular .
Disuse Atrophies .
Disuse Atrophy .
Muscular Atrophies, Spinobulbar .
Muscular Disorder, Atrophic .
Spinobulbar Atrophies .
Spinobulbar Muscular Atrophies .
Spinopontine Atrophies .
Atrophy, Disuse .
Atrophy, Muscular, Spinobulbar .
Atrophy, Spinopontine .
Muscular Atrophy, Spinobulbar .
Spinobulbar Muscular Atrophy .
Disorders characterized by an abnormal reduction in muscle volume due to a decrease in the size or number of muscle fibers. Atrophy may result from diseases intrinsic to muscle tissue (e.g., MUSCULAR DYSTROPHY) or secondary to PERIPHERAL NERVOUS SYSTEM DISEASES that impair innervation to muscle tissue (e.g., MUSCULAR ATROPHY, SPINAL). .
1.00
3356
 
Spinocerebellar Ataxias .
Autosomal Dominant Cerebellar Ataxia, Type II .
Cerebellar Degeneration with Slow Eye Movements .
Cerebelloparenchymal Disorder I .
Dominantly-Inherited Spinocerebellar Ataxias .
Menzel Type OPCA .
OPCA with Macular Degeneration and External Ophthalmoplegia .
OPCA with Retinal Degeneration .
Olivopontocerebellar Atrophy 2 .
Olivopontocerebellar Atrophy I .
Olivopontocerebellar Atrophy II .
Olivopontocerebellar Atrophy III .
Olivopontocerebellar Atrophy IV .
Olivopontocerebellar Atrophy, Holguin Type .
SCA1 22058 .
Schut-Haymaker Type OPCA .
Spinocerebellar Ataxia 1 .
Spinocerebellar Ataxia 2 .
Spinocerebellar Ataxia 4 .
Spinocerebellar Ataxia 5 .
Spinocerebellar Ataxia 6 .
Spinocerebellar Ataxia 7 .
Spinocerebellar Ataxia with Slow Eye Movements .
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy .
Spinocerebellar Ataxia, Cuban Type .
Spinocerebellar Ataxia-1 .
Spinocerebellar Ataxia-2 .
Spinocerebellar Ataxia-4 .
Spinocerebellar Ataxia-5 .
Spinocerebellar Ataxia-6 .
Spinocerebellar Ataxia-7 .
Spinocerebellar Ataxias, Dominantly-Inherited .
Spinocerebellar Atrophy 2 .
Spinocerebellar Atrophy I .
Spinocerebellar Atrophy II .
Spinocerebellar Degeneration with Slow Eye Movements .
Type 1 Spinocerebellar Ataxia .
Type 2 Spinocerebellar Ataxia .
Type 4 Spinocerebellar Ataxia .
Type 5 Spinocerebellar Ataxia .
Type 6 Spinocerebellar Ataxia .
Type 7 Spinocerebellar Ataxia .
Wadia Swami Syndrome .
Wadia-Swami Syndrome .
Ataxia 1, Spinocerebellar .
Ataxia 2, Spinocerebellar .
Ataxia 2s, Spinocerebellar .
Ataxia 4, Spinocerebellar .
Ataxia 4s, Spinocerebellar .
Ataxia 5, Spinocerebellar .
Ataxia 5s, Spinocerebellar .
Ataxia 6, Spinocerebellar .
Ataxia 6s, Spinocerebellar .
Ataxia 7, Spinocerebellar .
Ataxia 7s, Spinocerebellar .
Ataxia, Dominantly-Inherited Spinocerebellar .
Ataxia, Spinocerebellar .
Ataxias, Dominantly-Inherited Spinocerebellar .
Ataxias, Spinocerebellar .
Atrophies, Spinocerebellar .
Atrophy 2, Olivopontocerebellar .
Atrophy 2, Spinocerebellar .
Atrophy 2s, Olivopontocerebellar .
Atrophy 2s, Spinocerebellar .
Atrophy I, Olivopontocerebellar .
Atrophy I, Spinocerebellar .
Atrophy II, Olivopontocerebellar .
Atrophy II, Spinocerebellar .
Atrophy III, Olivopontocerebellar .
Atrophy IIs, Olivopontocerebellar .
Atrophy IIs, Spinocerebellar .
Atrophy IV, Olivopontocerebellar .
Atrophy IVs, Olivopontocerebellar .
Atrophy, Spinocerebellar .
Cerebelloparenchymal Disorder Is .
Dominantly Inherited Spinocerebellar Ataxias .
Dominantly-Inherited Spinocerebellar Ataxia .
II, Olivopontocerebellar Atrophy .
II, Spinocerebellar Atrophy .
IIs, Olivopontocerebellar Atrophy .
IIs, Spinocerebellar Atrophy .
OPCA, Menzel Type .
OPCA, Schut-Haymaker Type .
Olivopontocerebellar Atrophy 2s .
Olivopontocerebellar Atrophy IIIs .
Olivopontocerebellar Atrophy IIs .
Olivopontocerebellar Atrophy IVs .
Olivopontocerebellar Atrophy Is .
SCA1s .
Schut Haymaker Type OPCA .
Spinocerebellar Ataxia .
Spinocerebellar Ataxia 1s .
Spinocerebellar Ataxia 2s .
Spinocerebellar Ataxia 4s .
Spinocerebellar Ataxia 5s .
Spinocerebellar Ataxia 6s .
Spinocerebellar Ataxia 7s .
Spinocerebellar Ataxia, Dominantly-Inherited .
Spinocerebellar Ataxias, Dominantly Inherited .
Spinocerebellar Atrophy .
Spinocerebellar Atrophy 2s .
Spinocerebellar Atrophy IIs .
Spinocerebellar Atrophy Is .
Swami Syndrome, Wadia .
Syndrome, Wadia Swami .
Syndrome, Wadia-Swami .
Spinocerebellar Ataxia Type 1 .
Spinocerebellar Ataxia Type 2 .
Spinocerebellar Ataxia Type 4 .
Spinocerebellar Ataxia Type 5 .
Spinocerebellar Ataxia Type 6 .
Spinocerebellar Ataxia Type 7 .
Spinocerebellar Atrophies .
A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) .
0.68
511952
 
Atrophy .
Atrophies .
Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. .
0.66
32226073
 
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) .
0.60
8174