An infant with congenital heart defects and proteinuria: a case report

BACKGROUND: Branchio-Oto-Renal (BOR) Syndrome is a rare autosomal disorder with a wide variety of clinical manifestations and a high degree of heterogeneity. Typical clinical manifestations of BOR syndrome include deafness, preauricular fistula, abnormal gill slits, and renal malformations. However,...

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Detalles Bibliográficos
Autores principales: Liu, Dandan, Wang, Yafeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635197/
https://www.ncbi.nlm.nih.gov/pubmed/36333735
http://dx.doi.org/10.1186/s12887-022-03705-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635197/
https://www.ncbi.nlm.nih.gov/pubmed/36333735
http://dx.doi.org/10.1186/s12887-022-03705-4

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