Autosomal recessive spastic paraplegia type 27

Get in touch with RARE Concierge.

Contact RARE Concierge

Autosomal recessive spastic paraplegia type 27

Synonyms: SPG27

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.

Reference: Access aggregated data from Orphanet at Orphadata.

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?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Clinical Trials

For a list of clinical trials in this disease area, please click here.