Familial chylomicronemia syndrome: A rare but devastating autosomal recessive disorder characterized by refractory hypertriglyceridemia and recurrent pancreatitis-Reference-Cited by-同舟云学术

Familial chylomicronemia syndrome: A rare but devastating autosomal recessive disorder characterized by refractory hypertriglyceridemia and recurrent pancreatitis

Published:2020-02 Issue:2 Volume:30 Page:80-85
ISSN:1050-1738
Container-title:Trends in Cardiovascular Medicine
language:en
Short-container-title:Trends in Cardiovascular Medicine

Author:

Chyzhyk Vadzim,Brown Alan S.^ORCID

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference34 articles.

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3. Chylomicronaemia–current diagnosis and future therapies;Brahm;Nat Rev Endocrinol,2015

4. Classification of hyperlipidaemias and hyperlipoproteinaemias;Beaumont;Bull World Health Organ,1970

5. The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management;Hegele;Lancet Diabetes Endocrinol,2014

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