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Gaucher disease in a patient with membranoproliferative glomerulonephritis: case report
BACKGROUND: Gaucher disease (GD) is a rare autosomal recessive inherited, lysosomal storage disoder that involves liver, spleen, lung, bone, bone marrow even central nervous. However, GD associated membranoproliferative glomerulonephritis (MPGN) is seldom reported. CASE PRESENTATION: Here we describ...
Autores principales: | Liang, Mengjun, Zhu, Shiyan, Liu, Shaoqin, Chen, Jianquan, Li, Danni, Luo, Chengzhi, Wang, Xiaowen, Jiang, Zongpei |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541703/ https://www.ncbi.nlm.nih.gov/pubmed/37773105 http://dx.doi.org/10.1186/s12882-023-03163-9 |
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