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

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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Bibliographic Details
Main Author: Zhang Hong-wen
Format: Article
Language:zho
Published: Editorial Department of Journal of Clinical Nephrology 2025-05-01
Series:Linchuang shenzangbing zazhi
Subjects:
Nephritis
Hereditary
Alport syndrome
Female
<italic>COL4A5</italic>
Compound heterozygous variation
Online Access:http://www.lcszb.com/thesisDetails#10.3969/j.issn.1671-2390.2025.05.015
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