Fast Facts: Familial Chylomicronemia Syndrome (PDF)

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. Table of Contents: •Terminology, etiology and pathophysiology •Diagnosis •Complications •Management and prevention •Research directions
 
Product Details

Publisher ‏ : ‎ S. Karger
Publication date ‏ : ‎ December 27,2021
Language ‏ : ‎ English
Screen Reader ‏ : ‎ Supported
Sticky notes ‏ : ‎ On Kindle Scribe