Article

Genetic analysis of Indian patients with steroid-resistant nephrotic syndrome in children

2023-06-23

Abstract excerpt

<title>Abstract</title> <p>Introduction: Steroid-resistant nephrotic syndrome (SRNS) children carry poor outcomes. In the hope of achieving remission, patients are frequently treated with repeated courses of steroids and other immunosuppressives. Patients with genetic mutations are usually steroid-resistant, except for a few patients. There is a paucity of data on genetic mutations in Indian children with SRNS. <...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: a8e5014d-f418-5473-934d-94d56ae356e8
DOI: 10.21203/rs.3.rs-3065501/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Genetic analysis of Indian patients with steroid-resistant nephrotic syndrome in childrenDOI 10.21203/rs.3.rs-3065501/v1Read

Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.Semantic proximity Read

Genetic tests in children with steroid-resistant nephrotic syndromeSemantic proximity Read

Molecular genetic analysis of Steroid Resistant Nephrotic Syndrome: Detection of a novel mutationSemantic proximity Read

Genetics of steroid-resistant nephrotic syndrome: a review of mutation spectrum and suggested approach for genetic testing.Semantic proximity Read

A multicenter study investigating the genetic analysis of childhood steroid-resistant nephrotic syndrome: Variants in COL4A5 may not be coincidental.Semantic proximity Read

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.Semantic proximity Read

Monogenic Causes Identified in 23.68% of Children with Steroid-Resistant Nephrotic Syndrome: A Single-Centre StudySemantic proximity Read

Targeted Next-Generation Sequencing in Brazilian Children With Nephrotic Syndrome Submitted to Renal Transplant.Semantic proximity Read

Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndromeSemantic proximity Read

The Frequency of Genetic Mutations in Pediatric Patients Diagnosed with Nephrotic Syndrome: A Single-Center Retrospective Study in Saudi Arabia.Semantic proximity Read

Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndromeSemantic proximity Read

Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.Semantic proximity Read