Spastic paraplegia 29

Alternate names

SPG29

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.

NIH genetic and rare disease info

NIH info on Spastic paraplegia 29

Spastic paraplegia 29 is a rare disease.

Resources

Frequently asked questions

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Rare diseases - Spastic paraplegia 29
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Spastic paraplegia 29
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