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A steady and catastrophic cardiac condition known as transthyretin amyloid cardiomyopathy (ATTR-CM) - A type of Cardiac Amyloidosis . The definition, epidemiology, afflicted population, pathogenesis, symptoms, subtypes, diagnosis and pharmaceutical therapeutic techniques are all covered in this article's thorough discussion of ATTR-CM.This article addresses the molecular processes which lead to transthyretin amyloid fibrils accumulating and depositing, as well as the damage that amyloid does to the structure and function of the heart.The underlying mutations, familial inheritance patterns, and the necessity of identifying and screening individuals who may be susceptible to this disease are all covered in the article.The diagnostic possibilities to determine ATTR-CM are outlined in the diagnosis section. To provide an in-depth review of therapeutic methods of management are put forward.
This comprehensive review is an informative tool for medical practitioners, researchers, and for those who want to learn about the management of ATTR-CM.
"Unfolding the Intricate Details of an Unspoken Threat - Transthyretin Amyloid Cardiomyopathy", International Journal of Science & Engineering Development Research (www.ijrti.org), ISSN:2455-2631, Vol.8, Issue 7, page no.400 - 404, July-2023, Available :http://www.ijrti.org/papers/IJRTI2307061.pdf
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2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator