Cargando…
Prevalence estimation of ATTRv in China based on genetic databases
Introduction: Amyloid transthyretin (ATTR) is divided into either hereditary (ATTRv) or sporadic (ATTRwt) and ATTRv is a rare hereditary disease transmitted as an autosomal dominant manner. Its global prevalence is traditionally estimated as 5,000 to 10,000 persons. However, it may be underestimated...
Autores principales: | Yongsheng, Zheng, Chong, Sun, Bingyou, Liu, Jianian, Hu, Haofeng, Chen, Chongbo, Zhao, Zhang, Victor Wei, Jie, Lin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133693/ https://www.ncbi.nlm.nih.gov/pubmed/37124609 http://dx.doi.org/10.3389/fgene.2023.1126836 |
Ejemplares similares
-
A TRPV4 mutation caused Charcot-Marie-Tooth disease type 2C with scapuloperoneal muscular atrophy overlap syndrome and scapuloperoneal spinal muscular atrophy in one family: a case report and literature review
por: Chen, Haofeng, et al.
Publicado: (2023) -
Case Report: Hereditary transthyretin (ATTRv) amyloidosis: The p.G103R mutation of the transthyretin gene in a Han Chinese family is associated with vitreous hemorrhage
por: Shen, Junhui, et al.
Publicado: (2022) -
Clinical profile of autoimmune nodopathy with anti‐neurofascin 186 antibody
por: Liu, Bingyou, et al.
Publicado: (2023) -
ATTRv in Lazio-Italy: A High-Prevalence Region in a Non-Endemic Country
por: Luigetti, Marco, et al.
Publicado: (2021) -
Disease risk estimates in V30M variant transthyretin amyloidosis (A-ATTRv) from Mallorca
por: Cisneros-Barroso, E., et al.
Publicado: (2023)