Fabry Disease with Pacemaker Implantation as the Initial Event

Fabry disease (FD) is a rare X-linked hereditary disorder (Xq22) caused by a deficiency in alpha-galactosidase activity. A 34-year-old man was referred to our hospital because of renal dysfunction. He had previously undergone pacemaker implantation at 24 years of age. Investigations revealed undetec...

Descripción completa

Detalles Bibliográficos
Autores principales: Kato, Yuji, Ishikawa, Ayako, Aoki, Satoshi, Sato, Hiroyuki, Ojima, Yoshie, Kagaya, Saeko, Nagasawa, Tasuku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859394/
https://www.ncbi.nlm.nih.gov/pubmed/31243236
http://dx.doi.org/10.2169/internalmedicine.2468-18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859394/
https://www.ncbi.nlm.nih.gov/pubmed/31243236
http://dx.doi.org/10.2169/internalmedicine.2468-18

Ejemplares similares