Fig. 1From: Clinical features and molecular genetic investigation of infantile-onset ascending hereditary spastic paralysis (IAHSP) in two Chinese siblings caused by a novel splice site ALS2 variationThe clinical features of the patient with Infantile-onset ascending hereditary spastic paralysis. A-DÂ show the phenotypic characteristics of sister; E-HÂ show the phenotypic characteristics of brother: astasia, inability to walk, scoliosis, contracture of joint,lower limb hypertonia, foot pronationBack to article page