Alport syndrome misdiagnosed with IgA nephropathy from familial history: a case report and brief review

BACKGROUND: Alport syndrome is a rare inherited disease resulting from a primary disorder of the glomerular basement membrane. This disease results from mutations in genes encoding alpha chains of type IV collagen. In the differential diagnosis of this disease, IgA nephropathy is the most common pri...

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Detalles Bibliográficos
Autores principales: Rahimzadeh, Hormat, Ajlou, Sanaz, Nili, Fatemeh, Razeghi, Effat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105455/
https://www.ncbi.nlm.nih.gov/pubmed/37059980
http://dx.doi.org/10.1186/s12882-023-03165-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105455/
https://www.ncbi.nlm.nih.gov/pubmed/37059980
http://dx.doi.org/10.1186/s12882-023-03165-7

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