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Fig. 1 | BMC Medical Genomics

Fig. 1

From: 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 variation

Fig. 1

The clinical features of the patient with Infantile-onset ascending hereditary spastic paralysis. A-D show the phenotypic characteristics of sister; E-H show the phenotypic characteristics of brother: astasia, inability to walk, scoliosis, contracture of joint,lower limb hypertonia, foot pronation

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BMC Medical Genomics

ISSN: 1755-8794

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