Autosomal dominant spastic paraplegia type 42 (Q100876): Difference between revisions
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Paraplegia espástica autossômica dominante caracterizada por paraplegia espástica lentamente progressiva das extremidades inferiores com idade de início que varia desde a infância até a idade adulta. Os pacientes apresentam marcha espástica, aumento dos reflexos tendinosos nos membros inferiores, resposta extensora plantar, fraqueza e atrofia dos músculos dos membros inferiores e, raramente, pés cavos. | |||
| description / en | description / en | ||
Autosomal dominant spastic paraplegia characterized by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood. Patients present with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and rarely, pes cavus. | |||
Revision as of 17:39, 16 August 2026
Autosomal dominant spastic paraplegia characterized by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood. Patients present with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and rarely, pes cavus.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_661411419 |
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| English | Autosomal dominant spastic paraplegia type 42 |
Autosomal dominant spastic paraplegia characterized by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood. Patients present with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and rarely, pes cavus. |
