نتایج جستجو برای: idiopathic minimal change nephrotic syndrome

تعداد نتایج: 1372553  

Journal: :modares journal of medical sciences: pathobiology 2007
maryam keshavarz farideh khosravy behrouz nikbin malektaj honarmand abdolfatah sarafnejad

objectives: the idiopathic minimal change nephritic syndrome (nephrosis) is responsible in 80% of nephritic syndromes in children. it is a clinical entity characterized by inter and outer renal parameters. main factor in glomerolar damages is proteinuria and the role of ige is possible. aim: in this research, serum ige concentrations were measured in children with nephrosis in three stages: rel...

2013
Yonghui Xia Jianhua Mao Xia Jin Wenjing Wang Lizhong Du Aimin Liu

OBJECTIVES Familial steroid-sensitive idiopathic nephrotic syndrome is rare, and only approximately 3% of patients have affected siblings. METHODS Herein, we report seven cases of patients with steroid-sensitive idiopathic nephrotic syndrome from three Chinese families. Mutational screening of the Nphs2 gene was performed in all the patients. RESULTS All seven of the familial steroid-sensit...

سلیمانی, اکرم , سیدزاده, سیدابوالحسن , علیمحمدی, احسان ,

    Background & Aims : Nephrotic syndrome is one of the important diseases of childhood. Although physiopathology of the disease is not well understood but vast majority of patients have a benign course with good response to steroids. In this retrospective study, we reviewed clinical feature and course of 104 children with idiopathic nephrotic syndrome during 2001-2011 .   Materials & Methods ...

2016

Methods: The aim of this study was to assess the correlation between serum albumin level and ionized calcium in children with idiopathic nephrotic syndrome. An analytic study with cross sectional comparative design was applied to nephrotic syndrome and healthy children between 2-8 years old in the Department of Pediatric Nephrlology, Comilla Medical College Hospital. A total of 120 subjects wer...

2012
Luciana dos Santos Henriques Fabíola de Marcos Matos Maria Helena Vaisbich

OBJECTIVE We present a prospective study of a microemulsion of cyclosporin to treat idiopathic nephrotic syndrome in ten children with normal renal function who presented cyclosporin trough levels between 50 and 150 ng/ml and achieved complete remission with cyclosporin. To compare the pharmacokinetic parameters of cyclosporin in idiopathic nephrotic syndrome during remission and relapse of the...

Journal: :Lancet 2003
Allison A Eddy Jordan M Symons

Childhood nephrotic syndromes are most commonly caused by one of two idiopathic diseases: minimal-change nephrotic syndrome (MCNS) and focal segmental glomerulosclerosis (FSGS). A third distinct type, membranous nephropathy, is rare in children. Other causes of isolated nephrotic syndrome can be subdivided into two major categories: rare genetic disorders, and secondary diseases associated with...

2015
Giles Walters Faisal A. Choudhury Budhima Nanayakkara

The treatment of primary nephrotic syndrome such as minimal change nephropathy, membranous nephropathy, and focal segmental glomerulosclerosis nephropathy remains challenging. Whilst most cases of idiopathic nephrotic syndrome respond to steroid therapy and experience a limited number of relapses prior to complete remission, some cases suffer from frequent relapses and become steroid dependent ...

2017
Samuel N Uwaezuoke

Two histological subtypes of idiopathic nephrotic syndrome are commonly recognized in children, namely minimal change nephropathy and focal segmental glomerulosclerosis. Children with minimal change nephropathy (the majority of whom are steroid-sensitive) and focal segmental glomerulosclerosis (the majority of whom are steroid-resistant) require early identification in order to ensure appropria...

1997
Kook-Hwan Oh C Ahn JH Park JE Oh HJ Chin JS Han S Kim JG Chi MH Park JS Lee

We present a 30-year-old male patient who was initially diagnosed as minimal change nephrotic syndrome, 5 years later, the patient developed a localized form of idiopathic retroperitoneal fibrosis (IRF). An elevated ESR and concomitant nephrotic syndrome in the patient suggested the immunologic nature of IRF, IRF has been reported in association with collagen diseases and rarely with proliferat...

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