Fever, pulmonary interstitial fibrosis, and hepatomegaly in a 15-year-old boy with Gaucher disease: a case report

BACKGROUND: Gaucher disease is an autosomal recessive disorder resulting from the accumulation of glucocerebroside in the cells of the macrophage-monocyte system caused by deficiency in lysosomal glucocerebrosidase. Intravenously administered enzyme replacement therapy is the first-line therapy for...

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Detalles Bibliográficos
Autor principal: Yang, Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196019/
https://www.ncbi.nlm.nih.gov/pubmed/30342532
http://dx.doi.org/10.1186/s13256-018-1848-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196019/
https://www.ncbi.nlm.nih.gov/pubmed/30342532
http://dx.doi.org/10.1186/s13256-018-1848-z

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