- Transthyretin Amyloid Cardiomyopathy (ATTR-CM) - American Heart Association
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an underdiagnosed and potentially fatal disease of the heart muscle As it progresses, the heart can become unable to adequately squeeze to pump blood out of the heart, ultimately leading to heart failure
- Transthyretin Amyloidosis (ATTR-CM): Types, Causes, Treatment
Transthyretin amyloidosis (ATTR-CM) is a buildup of faulty proteins (fibrils) on your heart or nerves It can cause cardiomyopathy and heart failure
- ATTR-CM: Symptoms, Causes, Types and Treatment - HealthCentral
ATTR-CM is a heart condition caused by abnormally shaped protein deposits Learn the causes, symptoms, treatments, and other facts and tips for living with this heart condition
- Transthyretin Amyloid Cardiomyopathy (ATTR-CM) - WebMD
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a serious heart condition Learn about with this condition overview
- What to Know About Transthyretin Amyloid Cardiomyopathy (ATTR-CM)
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a serious disease that affects the left ventricle of the heart Learn about symptoms and treatment
- What to know about transthyretin amyloid cardiomyopathy
What is ATTR-CM? Read on to learn more about this rare type of heart disease, including possible causes, different forms, symptoms, and treatments
- Familial amyloid cardiomyopathy - Wikipedia
Familial amyloid cardiomyopathy (FAC), or transthyretin amyloid cardiomyopathy (ATTR-CM) results from the aggregation and deposition of mutant and wild-type transthyretin (TTR) protein in the heart [1] TTR is usually circulated as a homo-tetramer—a protein made up of four identical subunits—however, in FAC populations, TTR dissociates from this typical form and misassembles into amyloid
- What Is ATTR-CM? | Diagnosis, Symptoms, Subtypes More
Delayed diagnosis of ATTR-CM prevents timely intervention and contributes to premature death Learn about diagnosis, symptoms, subtypes and more
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