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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| Autor principal: | |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Gandhara University
2025-12-01
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| Col·lecció: | Journal of Gandhara Medical and Dental Sciences |
| Matèries: | |
| Accés en línia: | http://jgmds.org.pk/index.php/JGMDS/article/view/791 |
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