Three cases of steroid resistant nephrotic syndrome associated with gene mutation of transient receptor potential cation channel 6(TRPC 6)in children
<正>原发性肾病综合征中大约有20%的患儿出现激素耐药,其中局灶节段硬化(focal segmental glomerulosclerosis,FSGS)是其主要的病理改变,且多发生于6岁前,并在10岁内进展为ESRD[1-2]。目前已明确多种基因的突变参与FSGS的形成,尤其是编码足细胞相关蛋白的单基因突变在其中发挥重要作用[3]。
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Chinês |
| Gepubliceerd in: |
Editorial Department of Journal of Clinical Nephrology
2020-01-01
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| Reeks: | Linchuang shenzangbing zazhi |
| Onderwerpen: | |
| Online toegang: | http://www.lcszb.com/thesisDetails?columnId=57906671&Fpath=home&index=0 |
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