Familial chylomicronemia syndrome : raising awareness of a rare genetic disease /

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Bibliographic Details
Author / Creator:Davidson, Michael, 1956- author.
Imprint:Abingdon, Oxford : S. Karger, 2022.
©2022
Description:1 online resource (72 pages) : color illustrations
Language:English
Series:Fast facts
Fast facts.
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/13367267
Hidden Bibliographic Details
Other authors / contributors:Benes, Lane, author.
Wierzbicki, Anthony S., author.
ISBN:331806985X
9783318069853
9783318069846
3318069841
Notes:Includes bibliographical references and index.
Online resource; title from electronic title page (S. Karger, January 5, 2022).
Summary:"Familial chylomicronemia syndrome (FCS) is an ultra-rare genetic disorder characterized by the abnormal build-up of chylomicrons, the largest type of lipoprotein, which transport dietary fat from the gut to the rest of the body. Patients with FCS often experience severe symptoms, the most feared of which is acute, potentially life-threatening, pancreatitis. This resource is intended to raise awareness of FCS among all members of the healthcare team who come into contact with patients with FCS, with the aim of earlier diagnosis and management, thus preventing some of the more devastating physical, neurological and cognitive symptoms of the disorder"--Publisher's description
Other form:Print version: Davidson, Michael, 1956- Familial chylomicronemia syndrome. Abingdon, Oxford, UK : Karger, 2022 9783318069846