Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis

BACKGROUND: Hereditary spastic paraplegia (HSP) is a rare genetic disorder associated with mutations in > 80 loci designated SPG (SPastic parapleGia). The phenotypic spectrum of HSP can extend to include other neurologic features, including movement disorders. Our aim was to investigate genotype–...

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Detalles Bibliográficos
Autores principales: Fereshtehnejad, Seyed-Mohammad, Saleh, Philip A., Oliveira, Lais M., Patel, Neha, Bhowmick, Suvorit, Saranza, Gerard, Kalia, Lorraine V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925593/
https://www.ncbi.nlm.nih.gov/pubmed/36441344
http://dx.doi.org/10.1007/s10072-022-06516-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925593/
https://www.ncbi.nlm.nih.gov/pubmed/36441344
http://dx.doi.org/10.1007/s10072-022-06516-8

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