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.
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spastic paraplegia-nephritis-deafness syndrome
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spastic paraplegia-neuropathy-poikiloderma syndrome
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spastic paraplegia-precocious puberty syndrome
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hereditary spastic paraplegia 17
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