Cargando…
An Isolated Case of Late-onset Amyloidogenic Transthyretin Type Familial Amyloid Polyneuropathy Associated with a Mutant Transthyretin Substituting Methionine for Valine at Position 30 Showing Latent Progressive Cardiac Involvement Confirmed by Serial Annual Electrocardiograms
Late-onset amyloidogenic transthyretin (ATTR) type familial amyloid polyneuropathy (FAP) shows features distinct from those of early-onset hereditary ATTR type FAP. We herein describe an asymptomatic 68-year-old man with late-onset ATTR type FAP whose serial annual electrocardiograms demonstrated pr...
Autores principales: | Sato, Chikako, Takaya, Tomofumi, Mori, Shumpei, Hasegawa, Kohei, Soga, Fumitaka, Tanaka, Hidekazu, Watanabe, Yoshiaki, Nishii, Tatsuya, Kono, Atsushi K., Morinaga, Yukiko, Ishibashi-Ueda, Hatsue, Hirata, Ken-ichi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337461/ https://www.ncbi.nlm.nih.gov/pubmed/28090046 |
Ejemplares similares
-
Amyloidogenicity assessment of transthyretin gene variants
por: Grether, Nicolai B., et al.
Publicado: (2022) -
Diagnostic and Treatment Approaches Involving Transthyretin in Amyloidogenic Diseases
por: Park, Gil Yong, et al.
Publicado: (2019) -
Oligomerization Profile of Human Transthyretin Variants with Distinct Amyloidogenicity
por: Frangolho, Ana, et al.
Publicado: (2020) -
Epidemiology of transthyretin familial amyloid polyneuropathy in Portugal
por: Inês, Mónica, et al.
Publicado: (2015) -
The rehabilitation in the management of Transthyretin Familial Amyloid Polyneuropathy
por: Morier, Agnès, et al.
Publicado: (2015)