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Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
BACKGROUND: Lysosomal acid lipase deficiency (LALD) is an autosomal recessive inborn error of lipid metabolism characterized by impaired lysosomal hydrolysis and consequent accumulation of cholesteryl esters and triglycerides. The phenotypic spectrum is diverse, ranging from severe, neonatal onset f...
Kaydedildi:
| Yayımlandı: | Orphanet J Rare Dis |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7041253/ https://ncbi.nlm.nih.gov/pubmed/32093730 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-1328-6 |
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