Cargando…
Distinguishing Lysosomal Acid Lipase Deficiency From Familial Hypercholesterolemia
Lysosomal acid lipase deficiency (LAL-D) is underrecognized because it manifests clinically with lipid and lipoprotein values similar to those observed in heterozygous familial hypercholesterolemia (FH). Although LAL-D is uncommon, understanding the differences between the 2 diseases has significant...
Autores principales: | Sheth, Sohum, Toth, Peter P., Baum, Seth J., Aggarwal, Monica |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589441/ https://www.ncbi.nlm.nih.gov/pubmed/37869222 http://dx.doi.org/10.1016/j.jaccas.2023.102023 |
Ejemplares similares
-
The Emerging Battle: Lysosomal Acid Lipase Deficiency vs Familial Hypercholesterolemia in Children
por: Saad, Michelle, et al.
Publicado: (2021) -
Early Discovery of Children With Lysosomal Acid Lipase Deficiency With the Universal Familial Hypercholesterolemia Screening Program
por: Sustar, Ursa, et al.
Publicado: (2022) -
Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum
por: Curiati, Marco Antonio, et al.
Publicado: (2018) -
Clinical Features of Lysosomal Acid Lipase Deficiency
por: Burton, Barbara K., et al.
Publicado: (2015) -
Hepatosteatosis from Lysosomal Acid Lipase Deficiency
por: Zandanell, Stephan, et al.
Publicado: (2018)