Catalog

Autosomal dominant spastic paraplegia type 19

No MMS code

Link to WHO Definition

Autosomal dominant spastic paraplegia type 19 – http://id.who.int/icd/entity/1020508875

Autosomal dominant spastic paraplegia associated with SPG19 gene that presents with slowly progressive spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction, and mild sensory and motor peripheral neuropathy.