Autosomal recessive spastic paraplegia type 26 (Q99392): Difference between revisions
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Latest revision as of 16:03, 16 August 2026
Autosomal recessive spastic paraplegia that is caused by mutations in the B4GALNT1 gene. Onset is within the first two decades of life. Clinical characteristics include lower extremity spasticity and weakness. Individuals with this disorder can also have neuropathy, intellectual disability, neuropathy, cerebellar signs, and extrapyramidal signs.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1151541328 |
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| English | Autosomal recessive spastic paraplegia type 26 |
Autosomal recessive spastic paraplegia that is caused by mutations in the B4GALNT1 gene. Onset is within the first two decades of life. Clinical characteristics include lower extremity spasticity and weakness. Individuals with this disorder can also have neuropathy, intellectual disability, neuropathy, cerebellar signs, and extrapyramidal signs. |
Statements
CID11:ID_1151541328
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dki-india-ID_1151541328
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Concluído
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15 August 2026
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