Hereditary spastic paraplegia 29

Autosomal dominant spastic paraplegia type 29 (SPG29) is a complex form of hereditary spastic paraplegia characterized by a spastic paraplegia presenting in adolescence, associated with the additional manifestations of sensorial hearing impairment due to auditory neuropathy and persistent vomiting due to a hiatal or paraesophageal hernia.

Also known as: SPG29, hereditary spastic paraplegia type 29, autosomal dominant spastic paraplegia type 29, spastic paraplegia 29, spastic paraplegia 29, autosomal dominant

14 clinical trials for this condition and its sub-types.