Frasier syndrome: a case report
<正>Frasier综合征（fraise syndrome,FS）是一种罕见的遗传性肾脏病,为常染色体显性遗传,与WT1基因突变有关,通常在2～6岁起病,该病罕见报道,本文回顾分析厦门大学附属成功医院近期收治的1例成人FS患者的临床资料,现报道如下。
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| Main Authors: | , , |
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| Format: | Article |
| Language: | zho |
| Published: |
Editorial Department of Journal of Clinical Nephrology
2021-01-01
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| Series: | Linchuang shenzangbing zazhi |
| Subjects: | |
| Online Access: | http://www.lcszb.com/thesisDetails?columnId=57905141&Fpath=home&index=0 |
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