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Identifying suspected familial chylomicronemia syndrome
Familial chylomicronemia syndrome (FCS) is a rare lipid disorder posing significant clinical burdens on patients. Due to its rarity, variety of presentations, and lack of universal diagnostic criteria, patients see an average of five physicians before diagnosis. We screened adults for a triglyceride...
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| Publicado no: | Proc (Bayl Univ Med Cent) |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5997083/ https://ncbi.nlm.nih.gov/pubmed/29904289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/08998280.2018.1463784 |
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