15-Year progression to liver cancer in the lack of treatment for lysosomal acid lipase deficiency: A case report

Lysosomal acid lipase deficiency (LAL-D) is a poorly diagnosed genetic disorder characterized by the accumulation of cholesteryl esters and triglycerides in many tissues, leading to dyslipidemia and cardiovascular complications. In the liver, deposits are found within hepatocytes and Kupffer cells,...

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Detalles Bibliográficos
Autores principales: Cunha-Silva, Marlone, de França, Eloy Vianey Carvalho, Veiga, Clauber Teles, Greca, Raquel Dias, de Moraes, Priscilla Brito Sena, de Campos Mazo, Daniel Ferraz, de Ataíde, Elaine Cristina, Perales, Simone Reges, Monici, Leonardo Trevizan, Sevá-Pereira, Tiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9439781/
https://www.ncbi.nlm.nih.gov/pubmed/36107601
http://dx.doi.org/10.1097/MD.0000000000030315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9439781/
https://www.ncbi.nlm.nih.gov/pubmed/36107601
http://dx.doi.org/10.1097/MD.0000000000030315

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