Autosomal recessive spastic paraplegia type 14 (Q99406): Difference between revisions

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Paraplegia espástica autossômica recessiva caracterizada por paraplegia espástica lentamente progressiva de membros inferiores, com início na idade adulta, apresentando marcha espástica, hiperreflexia e hipertonicidade leve de membros inferiores associada a incapacidade intelectual leve, agnosia visual, deficiência de memória de curto e longo prazo e neuropatia motor distal leve. Pés cavos bilaterais e respostas extensoras plantares também estão associadas.
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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.

Revision as of 16:04, 16 August 2026

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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    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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