Autosomal dominant spastic paraplegia type 5A

Engelsk navn: Autosomal recessive spastic paraplegia type 5A
Engelske synonym: SPG5A


Autosomal recessive spastic paraplegia type 5A is a form of hereditary spastic paraplegia characterized by either a pure phenotype of slowly progressive spastic paraplegia of the lower extremities with bladder dysfunction and pes cavus or a complex presentation with additional manifestations including cerebellar signs, nystagmus, distal or generalized muscle atrophy and cognitive impairment. Age of onset is highly variable, ranging from early childhood to adulthood. White matter hyperintensity and cerebellar and spinal cord atrophy may be noted, on brain magnetic resonance imaging, in some patients.

Fra Orphanet

ORPHA: 100986
Klassifiseringsnivå: Disorder
ICD-10: G11.4

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