Fast Facts: Familial Chylomicronemia Syndrome : Raising awareness of a rare genetic disease

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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Davidson, Michael H., Benes, Lane (Awdur), Wierzbicki, Anthony S. (Awdur)
Fformat: Livre numérique
Iaith:Anglais
Cyhoeddwyd: Basel : S. Karger 2021.
Basel :
Mynediad Ar-lein:https://www.karger.com/Book/Home/281554
Accès Université d'Orléans et IFPM
Nodyn: Karger Fast Facts
Autres localisations: Voir dans le Sudoc
Edition sous un autre format:• Fast Facts: Familial Chylomicronemia Syndrome, 9783318069846
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520 |a 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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700 1 |a Wierzbicki, Anthony S.  |4 aut 
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