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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| Language: | zho |
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Editorial Department of Journal of Clinical Nephrology
2021-01-01
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| Series: | Linchuang shenzangbing zazhi |
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| Online Access: | http://www.lcszb.com/thesisDetails?columnId=57905141&Fpath=home&index=0 |
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| author | Li Cai-feng Hu Yu-qing Liang Meng |
| author_facet | Li Cai-feng Hu Yu-qing Liang Meng |
| author_sort | Li Cai-feng |
| collection | DOAJ |
| description | <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。 |
| format | Article |
| id | doaj-art-5c8277ae7f904aefbf6d39af4c1884d8 |
| institution | DOAJ |
| issn | 1671-2390 |
| language | zho |
| publishDate | 2021-01-01 |
| publisher | Editorial Department of Journal of Clinical Nephrology |
| record_format | Article |
| series | Linchuang shenzangbing zazhi |
| spelling | doaj-art-5c8277ae7f904aefbf6d39af4c1884d82025-08-20T03:09:13ZzhoEditorial Department of Journal of Clinical NephrologyLinchuang shenzangbing zazhi1671-23902021-01-011055105757905141Frasier syndrome: a case reportLi Cai-fengHu Yu-qingLiang Meng<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。http://www.lcszb.com/thesisDetails?columnId=57905141&Fpath=home&index=0Frasier syndromeGlomerulosclerosis,focal segmentalPseudohermaphroditismWt1 gene |
| spellingShingle | Li Cai-feng Hu Yu-qing Liang Meng Frasier syndrome: a case report Linchuang shenzangbing zazhi Frasier syndrome Glomerulosclerosis,focal segmental Pseudohermaphroditism Wt1 gene |
| title | Frasier syndrome: a case report |
| title_full | Frasier syndrome: a case report |
| title_fullStr | Frasier syndrome: a case report |
| title_full_unstemmed | Frasier syndrome: a case report |
| title_short | Frasier syndrome: a case report |
| title_sort | frasier syndrome a case report |
| topic | Frasier syndrome Glomerulosclerosis,focal segmental Pseudohermaphroditism Wt1 gene |
| url | http://www.lcszb.com/thesisDetails?columnId=57905141&Fpath=home&index=0 |
| work_keys_str_mv | AT licaifeng frasiersyndromeacasereport AT huyuqing frasiersyndromeacasereport AT liangmeng frasiersyndromeacasereport |