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Case report: Multidisciplinary collaboration in diagnosis and treatment of child gaucher disease
Gaucher disease (GD) is an inherited lysosomal storage disease caused by mutations in the glucocerebrosidase gene. The decrease of glucocerebrosidase activity in lysosomes results in the accumulation of its substrate glucocerebroside in the lysosomes of macrophages in organs such as the liver, splee...
Autores principales: | Zhu, Jianfang, Sun, Yuxiao, Zheng, Weiyan, Wang, Chunlin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098188/ https://www.ncbi.nlm.nih.gov/pubmed/37063666 http://dx.doi.org/10.3389/fped.2023.1057574 |
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