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 h...

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Detalles Bibliográficos
Autores principales: Wang, Dahai, Shan, Chunrong, Jing, Xinxin, Zhang, Qiuye, Chang, Hong, Lin, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631998/
https://www.ncbi.nlm.nih.gov/pubmed/34858896
http://dx.doi.org/10.3389/fped.2021.678633

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631998/
https://www.ncbi.nlm.nih.gov/pubmed/34858896
http://dx.doi.org/10.3389/fped.2021.678633

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