Hereditary spastic paraplegia 29
Hereditary spastic paraplegia 29
Definition
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 hereditary spastic paraplegia type 29, SPG29 — per MONDO