Catalog

Autosomal dominant spastic paraplegia type 37

No MMS code

Link to WHO Definition

Autosomal dominant spastic paraplegia type 37 – http://id.who.int/icd/entity/1636862745

A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction.