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Fast Facts: Familial Chylomicronemia Syndrome: Raising Awareness of a Rare Genetic Disease

Davidson, Michael H
Fast Facts: Familial Chylomicronemia Syndrome: Raising Awareness of a Rare Genetic Disease Cover Image
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List Price:$25.00

Book Information
Edition: 1st
Publisher: Karger, S.,Ag Med & Sci
ISBN: 3-318-06984-1 (3318069841)
ISBN-13: 978-3-318-06984-6 (9783318069846)
Format: Low Page Count
Binding: Softcover
Copyright: 2021
Publish Date: 01/22
Weight: 0.27 Lbs.
Pages: 72
Subject Class: GEN (Genetics)
Return Policy: Returns accepted up to 90 days provided no other recalls or return restrictions apply.
Contributing Authors: View
 
Class Specifications
Discipline: Biochemistry
Subject Definition: Chylomicrons; Lipoproteins
NLM Class: QU 85
LC Class: QP552
Abstract: 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.
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