Clinical profile and molecular genetic analysis of alport syndrome in children: a single center experience
In this study, the most commonly observed mutation was glycine substitution. Additionally, patients exhibiting severe mutations showed an increased vulnerability to complications, including proteinuria, ocular lesions, and hearing impairment. Genetic testing emerged as a critical resource for diagnosing AS. Furthermore, early diagnosis is crucial for implementing an appropriate management plan and assessing the prognosis.
Authors
- Shuai Zhao (ORCID: https://orcid.org/0009-0004-7688-6730)
- Yan Zhang (ORCID: https://orcid.org/0000-0002-5027-6430)
- Yan Ma
- Lijun Liang (ORCID: https://orcid.org/0000-0001-9641-5910)
- Aqsa Ahmad
- Du Wangnan
Institutions
- Dalian Medical University (CN)
- Ningxia Medical University (CN)
- Ningxia Medical University General Hospital (CN)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2024-12-23
- DOI
- https://doi.org/10.3389/fped.2024.1487927
- Primary Topic
- Cell Adhesion Molecules Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00