Gait Characterization and Analysis of Hereditary Amyloidosis Associated with Transthyretin Patients: A Case Series

Hereditary amyloidosis associated with transthyretin (ATTRv), is a rare autosomal dominant disease characterized by length-dependent symmetric polyneuropathy that has gait impairment as one of its consequences. The gait pattern of V30M ATTRv amyloidosis patients has been described as similar to that...

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Detalles Bibliográficos
Autores principales: Vilas-Boas, Maria do Carmo, Fonseca, Pedro Filipe Pereira, Sousa, Inês Martins, Cardoso, Márcio Neves, Cunha, João Paulo Silva, Coelho, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320786/
https://www.ncbi.nlm.nih.gov/pubmed/35887731
http://dx.doi.org/10.3390/jcm11143967

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320786/
https://www.ncbi.nlm.nih.gov/pubmed/35887731
http://dx.doi.org/10.3390/jcm11143967

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