Spastic paraplegia 16: Difference between revisions
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Latest revision as of 06:19, 4 February 2025
Alternate names
SPG16
Definition
A complex, hereditary, spastic paraplegia characterized by delayed motor development, spasticity, and inability to walk, later progressing to quadriplegia, motor aphasia, bowel and bladder dysfunction. Patients also present with vision problems and mild intellectual disability. The disease affects only males.
NIH genetic and rare disease info
Spastic paraplegia 16 is a rare disease.
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Rare diseases - Spastic paraplegia 16
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Resources
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Spastic paraplegia 16
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