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Autosomal recessive spastic paraplegia type 75

ORPHA:459056· ICD-10 G11.4

Definition

A rare, complex hereditary spastic paraplegia characterized by an early onset and slow progression of spastic paraplegia associated with cerebellar signs, nystagmus, peripheral neuropathy, extensor plantar responses and borderline to mild intellectual disability. Additional features of hypo- or areflexia, mild upper limb involvement and significant visual impairment (optic atrophy, vision loss, astigmatism) have been reported.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal recessive
Age of onset
Childhood