Autosomal dominant spastic paraplegia type 29

Orpha code: 101009OMIM code: 609727

Definition

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.

Disease data
Classification

Disease

Synonyms
SPG29
SPG29
ORPHA code
101009
OMIM code
609727
ICD10 code
G11.4
ICD11 code
-

No additional description.

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