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CRD often presents with non-specific symptoms, resulting in delayed diagnosis which is established by genetic workup and histology from small intestinal biopsies. Despite being rare, CRD needs to be considered as one of the differential diagnoses after ruling out the more common causes of FTT.<\/jats:p>","DOI":"10.1136\/bcr-2023-256999","type":"journal-article","created":{"date-parts":[[2024,6,14]],"date-time":"2024-06-14T16:39:20Z","timestamp":1718383160000},"page":"e256999","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":1,"title":["Chylomicron retention disease: a rare aetiology of failure to thrive"],"prefix":"10.1136","volume":"17","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4566-5212","authenticated-orcid":false,"given":"Yojana","family":"Sunkoj","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zhongxin","family":"Yu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Adnan","family":"Altaf","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Saurabh","family":"Talathi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2024,5,14]]},"reference":[{"key":"2024061408573247000_17.5.e256999.1","doi-asserted-by":"crossref","first-page":"797","DOI":"10.1016\/j.jacl.2022.08.009","article-title":"Guidance for the diagnosis and treatment of Hypolipidemia disorders","volume":"16","author":"Bredefeld","year":"2022","journal-title":"J Clin Lipidol"},{"key":"2024061408573247000_17.5.e256999.2","doi-asserted-by":"crossref","first-page":"4","DOI":"10.1097\/MPG.0000000000003145","article-title":"Lipids responsible for intestinal or hepatic disorder: when to suspect a familial intestinal Hypocholesterolemia","volume":"73","author":"Sissaoui","year":"2021","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"2024061408573247000_17.5.e256999.3","doi-asserted-by":"publisher","DOI":"10.1097\/MOL.0000000000000578"},{"key":"2024061408573247000_17.5.e256999.4","doi-asserted-by":"crossref","DOI":"10.1186\/1750-1172-5-24","article-title":"Guidelines for the diagnosis and management of Chylomicron retention disease based on a review of the literature and the experience of two centers","volume":"5","author":"Peretti","year":"2010","journal-title":"Orphanet J Rare Dis"},{"key":"2024061408573247000_17.5.e256999.5","unstructured":"Burnett JR , Hooper AJ , Hegele RA , et al . 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