A Case Report of COL4A5 Gene Mutation Alport Syndrome in 2 Native African Children

A Case Report of COL4A5 Gene Mutation Alport Syndrome in 2 Native African Children

Alport syndrome is a heterogeneous genetic disease involving the basement membrane of the glomeruli, inner ear, retina, and lens capsule. It typically manifests as progressive glomerulopathy that frequently results in end-stage renal disease, high-tone sensorineural deafness, and ocular abnormalitie...

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Bibliographic Details
Main Authors: Emmanuel Oduware, Nosakhare Joyce Iduoriyekemwen, Michael Ibadin, Henry Aikhionbare
Format: Article
Language:English
Published: Karger Publishers 2021-10-01
Series:Case Reports in Nephrology and Dialysis
Subjects:
col4a5 gene mutation
children
alport syndrome
Online Access:https://www.karger.com/Article/FullText/519076

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