Concept information
Término preferido
Muscular Atrophy, Spinal
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Tipo
-
mesh:Descriptor
Definición
- A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
Concepto genérico
Conceptos específicos
Etiquetas alternativas
- Spinal Amyotrophy
- Spinal Muscular Atrophy
En otras lenguas
-
francés
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AS (Amyotrophie Spinale)
-
Atrophie musculaire progressive
URI
http://data.loterre.fr/ark:/67375/JVR-FKFV32QS-R
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