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Nephrotic Syndrome in a Child with Alport Syndrome: A Case Report and Literature Review

Abstract: Alport syndrome is a disorder affecting basement membranes in the glomeruli, cochlea, and eyes due to mutations in collagen IV genes (COL4A3, COL4A4, COL4A5). It exhibits genetic and phenotypic variability and can be inherited via X-linked, autosomal recessive, or autosomal dominant pa...

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Hovedforfatter: syed shah
Format: Artigo
Sprog:Inglês
Udgivet: Gandhara University 2025-12-01
Serier:Journal of Gandhara Medical and Dental Sciences
Fag:
Alport Syndrome
Collagen Type IV Genes
COL4A5
X-Linked
Sensorineural Hearing Loss
Nephrotic Syndrome
Online adgang:http://jgmds.org.pk/index.php/JGMDS/article/view/791
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