Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency | Orphanet Journal of Rare Diseases | Full Text

Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency | Orphanet Journal of Rare Diseases | Full Text

Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency

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 triglycer...

Authors:Amanda Barone Pritchard, Alanna Strong and Can Ficicioglu

Citation:Orphanet Journal of Rare Diseases 2020 15:58

Content type:Research

Published on: 24 February 2020

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