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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
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Medical Book House is the Best online medical books resource which serves medical professionals in providing Ebooks, video courses/ Lectures of all kinds in various languages on their demand at very reasonable prices.