Autosomal dominant spastic paraplegia type 42 (Q100876): Difference between revisions
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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 |
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| 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. |
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CID11:ID_661411419
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dki-india-ID_661411419
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