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Fast Facts: Familial Chylomicronemia Syndrome

Raising Awareness of a Rare Genetic Disease
Buch | Softcover
66 Seiten
2021
Karger, S (Verlag)
978-3-318-06984-6 (ISBN)
CHF 25,65 inkl. MwSt
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
Erscheinungsdatum
Zusatzinfo 9 fig., 9 in color, 9 tab.
Verlagsort Basel
Sprache englisch
Maße 148 x 210 mm
Gewicht 120 g
Themenwelt Medizinische Fachgebiete Innere Medizin Gastroenterologie
Schlagworte gastroenterology
ISBN-10 3-318-06984-1 / 3318069841
ISBN-13 978-3-318-06984-6 / 9783318069846
Zustand Neuware
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