Hereditary spastic paraplegia due to NIPA1 gene mutation: Case report
Introduction: Hereditary spastic paraplegia (HSP) is the term for a group of neurological disorders characterized by progressive spasticity and muscle weakness in the lower limbs. Its etiology is genetic and has been associated with mutations in more than 60 genes. HSP is rare and may be useful in...
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| Fformat: | Artigo |
| Iaith: | Inglês |
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Universidad Nacional de Colombia
2022-08-01
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| Cyfres: | Case Reports |
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| Mynediad Ar-lein: | https://revistas.unal.edu.co/index.php/care/article/view/90865 |
| Tagiau: |
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
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