An infant with congenital heart defects and proteinuria: a case report
Abstract 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....
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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BMC
2022-11-01
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| Series: | BMC Pediatrics |
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| Online Access: | https://doi.org/10.1186/s12887-022-03705-4 |