Autosomal recessive spastic paraplegia type 27
Autosomal recessive spastic paraplegia type 27 is a rare pure or complex hereditary spastic paraplegia characterized by a variable onset of slowly progressive lower limb spasticity hyperreflexia and extensor plantar responses that may be associated with sensorimotor polyneuropathy decreased vibration sense lower limb distal muscle wasting dysarthria and mild to moderate intellectual disability.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024
Newly diagnosed with
Autosomal recessive spastic paraplegia type 27?
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