Abstract
Hereditary transthyretin amyloidosis with polyneuropathy (ATTR-PN) is a rare and multisystemic disease. Scarce evidence about its economic burden has been published, especially regarding carriers and early stage patients. To characterize these populations, a descriptive study was developed in Spain. Secondary endpoints were estimation of the use and costs of healthcare resource utilization (HRU) and estimation of indirect costs from a societal perspective.
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