Wilms′ tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome

Wilms′ tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome

Background & objectives: Clinically, nephrotic syndrome (NS) is a diverse group of symptoms; about 20 per cent of NS cases are resistant to steroid treatment, and within ten years they progress to end-stage renal disease. The present study was undertaken to identify the mutations of Wilms′ tumou...

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Bibliographic Details
Main Authors: Aravind Selvin Kumar, R Srilakshmi, SMK Karthickeyan, K Balakrishnan, R Padmaraj, Prabha Senguttuvan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Indian Journal of Medical Research
Subjects:
Denys-Drash syndrome - focal segmental glomerulosclerosis - Frasier syndrome - Indian children - steroid-resistant nephrotic syndrome - Wilms′ tumour 1
Online Access:http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2016;volume=144;issue=2;spage=276;epage=280;aulast=Kumar

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http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2016;volume=144;issue=2;spage=276;epage=280;aulast=Kumar

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