AIMS. Hereditary transthyretin-related amyloidosis (h-ATTR) is a systemic infiltrative disease caused by a single amino acid mutation on the transthyretin (TTR) gene, which destabilizes the protein and can determine its deposition on multiple organs, including heart and peripheral nervous system. We...
(AL) amyloidosis", "correct": false}, {"text": "Multiple myeloma", "correct": false}, {"text": "Scleredema", "correct": false}, {"text": "Scleromyxedema", "correct": true}, {"text": "Systemic sclerosis", "correct": false}]} {"image_url": "https://csvc.nejm.org/Content...