Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation: A case report

RATIONALE: Hereditary amyloidosis is diagnosed worldwidely with an increasing incidence. As the most common form, transthyretin-related hereditary amyloidosis (ATTR amyloidosis) is an autosomal dominant inherited disease due to mutations of TTR. Over the past several decades, more than 130 mutations...

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Detalles Bibliográficos
Autores principales: Xu, Jing, Yang, Meng, Pan, Xiaoxia, Yu, Xialian, Xie, Jingyuan, Ren, Hong, Li, Xiao, Chen, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348144/
https://www.ncbi.nlm.nih.gov/pubmed/28272196
http://dx.doi.org/10.1097/MD.0000000000005737

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348144/
https://www.ncbi.nlm.nih.gov/pubmed/28272196
http://dx.doi.org/10.1097/MD.0000000000005737

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