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2020
November 2020
Amyloidosis News - November 2020
Wild-Type Transthyretin: More Than What Meets the Heart
Early Diagnosis
The neurologic features of patients with wild-type transthyretin are highlighted, and the variability and overlap of neurologic symptoms are categorized in this case review series.
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Transthyretin Cardiac Amyloidosis in the African-American Population
Hereditary ATTR
Focusing on the prevalence of the
Val122Ile
mutation in African-American patients with hereditary transthyretin cardiac amyloidosis may lead to underestimation of this condition in this population.
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Revealing Cardiac Amyloidosis Disguised as Hypertrophic Obstructive Cardiomyopathy
Misdiagnosis
This case study highlights the importance of selecting the appropriate imaging modality to diagnose cardiac amyloidosis.
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Guideline-Directed Medical Therapy May Not Be Harmful in Patients with TTR-CA and Heart Failure with Reduced Ejection Fraction
Clinical Management
In a select group of patients with transthyretin cardiac amyloidosis (TTR-CA) and heart failure with reduced ejection fraction, guideline-directed medical therapy may be beneficial.
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Patient and Family Experience of Transthyretin Amyloidosis: Results of 2 Focus Groups
Patient Journey and Experiences
Educating clinicians about transthyretin amyloidosis (ATTR) may help reduce the myriad of challenges and burdens faced by patients with ATTR and their families.
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