Patient Education
La AhTTR se debe a un cambio genetico (mutacion) que afecta a la funcion de una proteina en la sangre denominada transtiretina (TTR). Esta proteina se produce…
L'amylose hATTR est causee par la modification d'un gene (une mutation) affectant la fonction d'une proteine dans le sang appelee transthyretine (TTR). Cette…
A amiloidose ATTRh e provocada por uma alteracao genetica (mutacao) que afeta o funcionamento de uma proteina designada por transtirretina (TTR). Esta proteina e…
Adoptar habitos saludables sencillos representa uno de los factores mas infl uyentes en el desarrollo de una vida sana. El estado nutricional afecta a la salud…
Amyloidosis can be localized or systemic, and it can be acquired or genetically inherited. The most common types include AL, which is caused by the malformation or…
Transthyretin amyloidosis is a rare, progressive disease characterized by the abnormal buildup of amyloid deposits composed of misfolded transthyretin protein in…
Rare diseases present unique challenges, often beginning with a diagnosis. Symptoms may puzzle patients and even leave health care providers uncertain. Diagnostic…
Amyloidosis is a rare disease caused by a buildup of abnormal proteins in the body's organs and tissue. Diagnosing amyloidosis can be difficult because symptoms…
This broadcast was hosted by Dr. David Seldin. He was the director of Amyloid Treatment and Research program, Boston University School of Medicine. He talks about…
To diagnose amyloidosis, some major steps should be considered by the patients and healthcare professionals. The primary step of diagnosis is that the healthcare…