Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/235257
Type: Artigo de periódico
Title: Nphs1 Gene Mutations Confirm Congenital Nephrotic Syndrome In Four Brazilian Cases: A Novel Mutation Is Described.
Author: Guaragna, Mara S
Cleto, Thaís Lira
Souza, Marcela Lopes
Lutaif, Anna Cristina G B
de Castro, Luiz Cláudio Gonçalves
Penido, Maria Goretti Moreira Guimarães
Maciel-Guerra, Andréa T
Belangero, Vera M S
Guerra-Junior, Gil
De Mello, Maricilda P
Abstract: Autosomal recessive mutations in NPHS1 gene are a common cause of congenital nephrotic syndrome (CNS). The disorder is characterized by massive proteinuria that manifests in utero or in the neonatal period during the first 3 months of life. NPHS1 encodes nephrin, a member of the immunoglobulin family of cell adhesion molecules and the main protein expressed at the renal slit diaphragm. Currently, there are approximately 250 mutations described in NPHS1 gene distributed among all nephrin domains. The main objective of this study was to perform the analysis of NPHS1 gene in patients with congenital nephrotic syndrome in order to determine the molecular cause of the disease. We performed direct sequencing of NPHS1 gene in four children. Each patient was heterozygous for two pathogenic mutations disclosing the molecular cause of the disease in 100% of the cases. We identified six different mutations, consisting of one in-frame deletion, one frameshift, and four missense substitutions. The p.Val736Met mutation that is described here for the first time was considered pathogenic by different mutation predictive algorithms. Regardless of the type of mutation, three patients had a bad outcome and died. Despite the small size of the cohort, this study contributed to the increasing number of deleterious mutations in the NPHS1 gene by describing a new mutation. Also, since we identified NPHS1 pathogenic mutations as the cause of the disease in all cases analyzed, it might be a frequent cause of CNS in South Eastern region of Brazil, although the analysis of a larger sample is required to obtain more indicative epidemiological data.
Subject: Nphs1 Gene
Congenital Nephrotic Syndrome
Nephrin
Novel Mutation
Citation: Nephrology (carlton, Vic.). , 2015-Nov.
Rights: embargo
Identifier DOI: 10.1111/nep.12667
Address: http://www.ncbi.nlm.nih.gov/pubmed/26560236
Date Issue: 2015
Appears in Collections:Unicamp - Artigos e Outros Documentos

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