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Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis

التفاصيل البيبلوغرافية
العنوان: Hereditary Apolipoprotein A-I–Associated Cardiac Amyloidosis
المؤلفون: Md. Shahrier Amin, George Sokos, Christopher Bianco, Saira Farid, Maryam Saleem, Marco Caccamo, Sudarshan Balla
المصدر: JACC Case Reports
بيانات النشر: Elsevier BV, 2021.
سنة النشر: 2021
مصطلحات موضوعية: ATTR, amyloid transthyretin, Pathology, medicine.medical_specialty, HCM, hypertrophic cardiomyopathy, Apolipoprotein B, apolipoprotein, HFpEF, heart failure with preserved ejection fraction, Case Report, HCM - Hypertrophic cardiomyopathy, Endomyocardial biopsy, LC MS/MS, liquid chromatography tandem mass spectrometry, AApo A-I, amyloid apolipoprotein A-I, Clinical Case, CMR, cardiac magnetic resonance, medicine, infiltrative cardiomyopathy, CA, cardiac amyloidosis, biology, business.industry, Infiltrative cardiomyopathy, Amyloidosis, Diagnostic algorithms, medicine.disease, EMB - Endomyocardial biopsy, humanities, Cardiac amyloidosis, endomyocardial biopsy, EMB, endomyocardial biopsy, biology.protein, Cardiology and Cardiovascular Medicine, business, AL, immunoglobulin light chain
الوصف: Cardiac amyloidosis has recently garnered substantial attention. Although the advent of noninvasive diagnostic algorithms revolutionized diagnosis, endomyocardial biopsy may still be considered in select cases to determine the amyloidosis subtype definitively. We report a case of a patients with a known mutation causing hereditary apolipoprotein A-I–associated cardiac amyloidosis. (Level of Difficulty: Advanced.)
Central Illustration
تدمد: 2666-0849
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e48c94d0711f2c332f3a7591671c54
https://doi.org/10.1016/j.jaccas.2021.02.016
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....85e48c94d0711f2c332f3a7591671c54
قاعدة البيانات: OpenAIRE
الوصف
تدمد:26660849