Wild type transthyretin-related amyloid cardiomyopathy (Q86511): Difference between revisions

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Revision as of 11:55, 15 August 2026

Wild type transthyretin (TTR)-related amyloid cardiomyopathy is a non-hereditary sporadic TTR-related systemic amyloidosis with predominant cardiac involvement associated with advancing age and resulting from myocardial infiltration of misaggregated wild-type transthyretin into amyloid filaments.
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    Wild type transthyretin-related amyloid cardiomyopathy
    Wild type transthyretin (TTR)-related amyloid cardiomyopathy is a non-hereditary sporadic TTR-related systemic amyloidosis with predominant cardiac involvement associated with advancing age and resulting from myocardial infiltration of misaggregated wild-type transthyretin into amyloid filaments.

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      CID11:ID_25699053
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