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GENATLAS PHENOTYPE

last update : 23-05-2017

Symbol	SPG77
Location	6p25.1
Name	spastic paraplegia 77, autosomal recessive
Corresponding gene	FARS2
Main clinical features	early-childhood onset of spasticity affecting the lower limbs and resulting in gait difficulties; the disorder is slowly progressive slowly progressive lower limb spasticity, pyramidal weakness with hyperreflexia, and scissoring gait; brain imaging was normal
Genetic determination	autosomal recessive
Function/system disorder	neurology
Type	disease

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