Cargando…
Significant Quality of Life Improvement Observed in a Patient With FCS Associated With a Marked Reduction in Triglycerides
Familial chylomicronemia syndrome (FCS) is a rare genetic disorder characterized by severely high triglycerides (TGs). It is associated with a marked increase in risk of recurrent, potentially fatal acute pancreatitis (AP), and symptoms including abdominal pain, fatigue, and anxiety that may substan...
Autor principal: | Gouni-Berthold, Ioanna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025947/ https://www.ncbi.nlm.nih.gov/pubmed/32083235 http://dx.doi.org/10.1210/jendso/bvz035 |
Ejemplares similares
-
Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score
por: Moulin, Philippe, et al.
Publicado: (2018) -
Sustainability of FCs
por: Losito, Roberto
Publicado: (2023) -
Background Reduction
in STED-FCS Using a Bivortex
Phase Mask
por: Barbotin, Aurélien, et al.
Publicado: (2020) -
Developments of FCS-link interface cards
por: Rubin, G, et al.
Publicado: (1996) -
Measuring Mobility in Chromatin by Intensity-Sorted FCS
por: Di Bona, Melody, et al.
Publicado: (2019)