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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Autores principales: Dahai Wang, Chunrong Shan, Xinxin Jing, Qiuye Zhang, Hong Chang, Yi Lin
Formato: article
Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
Materias:
Alport syndrome
autosomal inheritance
COL4A4
nephrotic syndrome
end-stage renal disease
Pediatrics
RJ1-570
Acceso en línea:https://doaj.org/article/9365015f93d143ea87c6d54ffa9fb008
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