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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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Proc (Bayl Univ Med Cent)
Asıl Yazarlar: Rengarajan, Ronak, McCullough, Peter A., Chowdhury, Anima, Tecson, Kristen M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Taylor & Francis 2018
Konular:
Original Research
Online Erişim: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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