Maternally-inherited spastic paraplegia

MONDO:0017917

A rare, genetic, complex hereditary spastic paraplegia disorder characterized by adulthood-onset of slowly progressive, bilateral, mainly lower limb spasticity and distal weakness associated with lower limb pain, hyperreflexia, and reduced vibration sense. Axonal neuropathy is frequently observed on electromyography and nerve conduction examination.

Also known as: MT-ATP6-related mitochondrial spastic paraplegia, maternally-inherited SPG

2 clinical trials for this condition and its sub-types, 0 tagged with Maternally-inherited spastic paraplegia itself.

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↑ Complex hereditary spastic paraplegia (7)

Including sub-types (2) Tagged with Maternally-inherited spastic paraplegia (0)

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