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It is suggested that the diagnosis of this type is vital to prevent any therapy\u2010related complications when it is erroneously diagnosed as AL amyloidosis. The clinical presentation is usually slowly progressive kidney disease and mild hepatic impairment. We report a case of LECT2 amyloidosis, which presented with severe painless cholestasis and hepatic encephalopathy alongside progressive kidney disease.<\/jats:p>","DOI":"10.1002\/ccr3.5185","type":"journal-article","created":{"date-parts":[[2021,12,5]],"date-time":"2021-12-05T12:55:25Z","timestamp":1638708925000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Leukocyte chemotactic factor 2\u2013related amyloidosis presenting with severe jaundice and hepatic encephalopathy"],"prefix":"10.1002","volume":"9","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9549-8352","authenticated-orcid":false,"given":"Hussam","family":"Almasri","sequence":"first","affiliation":[{"name":"Department of Medicine Hamad Medical Corporation Doha Qatar"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Almurtada","family":"Razok","sequence":"additional","affiliation":[{"name":"Department of Medicine Hamad Medical 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