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...

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Detalles Bibliográficos
Autores principales: Liang, Mengjun, Zhu, Shiyan, Liu, Shaoqin, Chen, Jianquan, Li, Danni, Luo, Chengzhi, Wang, Xiaowen, Jiang, Zongpei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
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

Internet

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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