Screening program for familial hyperchylomicronemia syndrome detection: Experience of a university health system
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 program for FCS in Argentina. Materials and methods:...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Sociedade Brasileira de Endocrinologia e Metabologia
2023-02-01
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| Edice: | Archives of Endocrinology and Metabolism |
| Témata: | |
| On-line přístup: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972023005004306&tlng=en |
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