Autosomal recessive spastic paraplegia type 11

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Name:
Autosomal recessive spastic paraplegia type 11
Description:
A complex hereditary spastic paraplegia characterized by progressive lower limbs weakness and spasticity, upper limbs weakness, dysarthria, hypomimia, sphincter disturbances, peripheral neuropathy, learning difficulties, cognitive impairment and dementia. Magnetic resonance imaging shows thin corpus callosum, cerebral atrophy, and periventricular white matter changes.
ORPHAcode:
2822
Synonyms:
Nakamura-Osame syndrome
SPG11
Spastic paraplegia-intellectual disability-thin corpus callosum syndrome
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14