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Article

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

BMC pediatrics - 4 Nov 2022

Liu Dandan, Wang Yafeng

Abstract excerpt

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, atypical phenotypes such as congenital hip dysplasia, congenital heart anomaly or facial nerve paresis are rare in...

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Identifiers

PMID: 36333735
DOI: 10.1186/s12887-022-03705-4
PMCID: PMC9635197

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