Clinical Features and Familial Mutations in an Autosomal-Inherited Alport Syndrome Patient With the Presentation of Nephrotic Syndrome

Clinical Features and Familial Mutations in an Autosomal-Inherited Alport Syndrome Patient With the Presentation of Nephrotic Syndrome

Background: The aim of this study was to report the clinical features and mutations in a patient with autosomal-inherited Alport syndrome (AS).Methods: We examined the clinical data, mutation analysis results, and family tree of a patient with autosomal-inherited AS, who had nephrotic syndrome as he...

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Bibliographic Details
Main Authors: Dahai Wang, Chunrong Shan, Xinxin Jing, Qiuye Zhang, Hong Chang, Yi Lin
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-11-01
Series:Frontiers in Pediatrics
Subjects:
Alport syndrome
autosomal inheritance
COL4A4
nephrotic syndrome
end-stage renal disease
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.678633/full

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https://www.frontiersin.org/articles/10.3389/fped.2021.678633/full

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