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GENATLAS PHENOTYPE

last update : 06-01-2016

Symbol	SPG61
Location	16p12.3
Name	Spastic paraplegia 61
Corresponding gene	ARL6IP1
Main clinical features	complicated form of spastic paraplegia with sensory and motor polyneuropathy, without mental retardation early inability to walk unsupported and with a scissors gait.; difficulty walking with support and spasticity with increased patellar and absent Achilles tendon reflexes as well as diffuse polysensory and motor neuropathy with loss of terminal digits and acropathy
Genetic determination	autosomal recessive
Function/system disorder	neurology
Type	disease

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