Autosomal recessive spastic paraplegia type 27 (Q99395)

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Hereditary spastic paraplegia characterized by 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.
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    Autosomal recessive spastic paraplegia type 27
    Hereditary spastic paraplegia characterized by 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.

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