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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,...
Autores principales: | Liu, Dandan, Wang, Yafeng |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
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 |
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