Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review
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| Format: | Article |
| Language: | zho |
| Published: |
Editorial Department of Journal of Clinical Nephrology
2025-05-01
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| Series: | Linchuang shenzangbing zazhi |
| Subjects: | |
| Online Access: | http://www.lcszb.com/thesisDetails#10.3969/j.issn.1671-2390.2025.05.015 |
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| _version_ | 1850240839454818304 |
|---|---|
| author | Zhang Hong-wen |
| author_facet | Zhang Hong-wen |
| author_sort | Zhang Hong-wen |
| collection | DOAJ |
| format | Article |
| id | doaj-art-6ec0de54ccd44c76b6793bcec3f0bbbf |
| institution | OA Journals |
| issn | 1671-2390 |
| language | zho |
| publishDate | 2025-05-01 |
| publisher | Editorial Department of Journal of Clinical Nephrology |
| record_format | Article |
| series | Linchuang shenzangbing zazhi |
| spelling | doaj-art-6ec0de54ccd44c76b6793bcec3f0bbbf2025-08-20T02:00:46ZzhoEditorial Department of Journal of Clinical NephrologyLinchuang shenzangbing zazhi1671-23902025-05-0125436438104262652Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature reviewZhang Hong-wenhttp://www.lcszb.com/thesisDetails#10.3969/j.issn.1671-2390.2025.05.015NephritisHereditaryAlport syndromeFemale<italic>COL4A5</italic>Compound heterozygous variation |
| spellingShingle | Zhang Hong-wen Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review Linchuang shenzangbing zazhi Nephritis Hereditary Alport syndrome Female <italic>COL4A5</italic> Compound heterozygous variation |
| title | Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review |
| title_full | Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review |
| title_fullStr | Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review |
| title_full_unstemmed | Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review |
| title_short | Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review |
| title_sort | severe clinical phenotype caused by the italic col4a5 italic compound heterozygous variation in a female patient with x linked dominant inheritance alport syndrome a case report and literature review |
| topic | Nephritis Hereditary Alport syndrome Female <italic>COL4A5</italic> Compound heterozygous variation |
| url | http://www.lcszb.com/thesisDetails#10.3969/j.issn.1671-2390.2025.05.015 |
| work_keys_str_mv | AT zhanghongwen severeclinicalphenotypecausedbytheitaliccol4a5italiccompoundheterozygousvariationinafemalepatientwithxlinkeddominantinheritancealportsyndromeacasereportandliteraturereview |