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A338 LYSOSOMAL ACID LIPASE DEFICIENCY (LAL-D): FROM DIAGNOSIS TO THERAPY IN CANADA
BACKGROUND: Lysosomal Acid Lipase (LAL-D) deficiency is an ultra-rare lysosomal storage disorder. Clinical features in the late-onset form include dyslipidemia (elevated LDL, low HDL), elevated liver enzymes, hepatomegaly, and splenomegaly. This can progress to liver fibrosis and cirrhosis. LAL-D is...
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| Publicado no: | J Can Assoc Gastroenterol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6508349/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jcag/gwy009.338 |
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