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Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome

1 Dec 2018

Abstract excerpt

BACKGROUND: Congenital nephrotic syndrome (CNS) is characterised by increased proteinuria, hypoproteinemia, and edema beginning in the first 3 months of life. Recently, molecular genetic studies have identified several genes involved in the pathogenesis of CNS. A systematic investigation of the genes for CNS in China has never been performed; therefore, we conducted a mutational analysis in 12 children with...

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PMID: 30594156
DOI: 10.1186/s12882-018-1184-y

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