Screening program for familial hyperchylomicronemia syndrome detection: Experience of a university health system.
Sign Up to like & getrecommendations! Published in 2023 at "Archives of endocrinology and metabolism"
DOI: 10.20945/2359-3997000000601
Abstract: ABSTRACT Objective: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive metabolic disorder caused by mutations related to chylomicron metabolism. The objective of this study is to show the development and results of a screening… read more here.
Keywords: screening program; suspected laboratory; program; detection ... See more keywords