Autosomal recessive spastic paraplegia type 14 (Q99406)

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Autosomal recessive spastic paraplegia characterized by adulthood-onset of slowly progressive spastic paraplegia of lower limbs presenting with spastic gait, hyperreflexia, and mild lower limb hypertonicity associated with mild intellectual disability, visual agnosia, short and long-term memory deficiency, and mild distal motor neuropathy. Bilateral pes cavus and extensor plantar responses are also associated.
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ID_1304184567
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    Autosomal recessive spastic paraplegia type 14
    Autosomal recessive spastic paraplegia characterized by adulthood-onset of slowly progressive spastic paraplegia of lower limbs presenting with spastic gait, hyperreflexia, and mild lower limb hypertonicity associated with mild intellectual disability, visual agnosia, short and long-term memory deficiency, and mild distal motor neuropathy. Bilateral pes cavus and extensor plantar responses are also associated.

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      CID11:ID_1304184567
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      dki-india-ID_1304184567
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