IgA肾病发病机制研究纵览
<正>IgA肾病是1968年由法国学者Berger和Hinglais首先描述和命名的,因此也称为Berger病,该病早期主要病理变化为多聚体低糖基化IgA1免疫复合物(polymer galactose-deficient IgA1 immune complexes,pGd-IgA1-IC)在肾小球系膜区沉积。IgA肾病是世界范围内公认最常见的原发性肾小球疾病,在我国也是导致终末期肾脏疾病最常见的病...
Saved in:
| Main Authors: | 李慧琼, 刘帝, 刘烨歆, 谭夏, 贺理宇, 王畅, 刘虹 |
|---|---|
| Format: | Article |
| Language: | zho |
| Published: |
Editorial Department of Journal of Clinical Nephrology
2016-01-01
|
| Series: | Linchuang shenzangbing zazhi |
| Online Access: | http://www.lcszb.com/thesisDetails?columnId=57918132&Fpath=home&index=0 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
IgA肾病发病机制的相关研究进展
by: 王菲菲, et al.
Published: (2024-01-01) -
特发性膜性肾病发病机制的研究进展
by: 吴成态, et al.
Published: (2018-01-01) -
小儿微小病变肾病综合征免疫发病机制研究进展
Published: (2013-01-01) -
诊断Fabry病合并IgA肾病2例
by: 李勰家, et al.
Published: (2018-01-01) -
补体活化异常在IgA肾病致病机制中的研究进展
by: 黄世雪, et al.
Published: (2018-01-01)