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Hereditary spastic paraplegia 19

MONDO:0011785

Autosomal dominant spastic paraplegia type 19 is a pure form of hereditary spastic paraplegia characterized by a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy.

Also known as: SPG19, autosomal dominant spastic paraplegia type 19, hereditary spastic paraplegia type 19, spastic paraplegia 19, spastic paraplegia 19, autosomal dominant

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 19 itself.

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