Clinical profile and molecular genetic analysis of alport syndrome in children: a single center experience

Clinical profile and molecular genetic analysis of alport syndrome in children: a single center experience

BackgroundAlport syndrome (AS) is a multifaceted condition that primarily affects the basement membranes of the kidneys, ears, and eyes. AS is considered the second most common cause of hereditary renal failure, exhibiting varied clinical manifestations across different lifespans. The aim of this st...

Full description

Saved in:
Bibliographic Details
Main Authors: Aqsa Ahmad, Liang Lijun, Zhang Yan, Ma Yan, Zhao Shuai, Du Wangnan
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-12-01
Series:Frontiers in Pediatrics
Subjects:
alport syndrome
clinical features
genetic testing
hematuria
children
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2024.1487927/full
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items

Similar Items