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Fast facts: familial chylomicronemia syndrome : raising awareness of a rare genetic disease

Michael H. Davidson, Lane Benes, Anthony S. Wierzbicki

Publikováno
Basel : S. Karger, 2021
Stránkování
72 stran : ilustrace, tabulky

Jazyk angličtina Země Německo

Typ dokumentu příručky

Perzistentní odkaz   https://www.medvik.cz/link/krg281554
E-zdroje
Odkazy

Knihovny.cz ISBN 9783318069853
plný text - pouze pro uživatele NLK Karger Fast Facts e-book
Knihovny.cz E-zdroje

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

Familial chylomicronemia syndrome

Print version:

Fast Facts: Familial Chylomicronemia Syndrome. ISBN 9783318069846 Knihovny.cz

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Print version record

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