نتایج جستجو برای: resistant nephrotic syndrome

تعداد نتایج: 804441  

Journal: :journal of pediatrics review 0
hamid mohammadjafari molecular and cell biology research center, department of pediatric nephrology, faculty of medicine, mazandaran university of medical sciences, sari, iran ahmadali nikibakhsh nephrology and transplantation research center, faculty of medicine, urmia university of medical sciences, urmia, iran abbas alipour department of community medicine, faculty of medicine, mazandaran university of medical sciences, sari, iran

corticosteroid resistant and dependent nephrotic syndrome in children is a challenge and there are some difficulties in treating such patients. we reviewed the current studies that evaluated therapeutic role of a relatively new immunosuppressive drug “rituximab” in reducing proteinuria and reduction of relapse rate in less than 16 year old patients with non-responsive or steroid dependent nephr...

Journal: :international journal of pediatrics 0
rahime renda antalya research and education hospital, pediatric nephrology department, antalya, turkey. özlem aydoğ ankara dr.sami ulus research and education hospital, pediatric nephrology department, ankara, turkey. mehmet bülbül ankara dr.sami ulus research and education hospital, pediatric nephrology department, ankara, turkey. evrim kargın çakıcı ankara dr.sami ulus research and education hospital, pediatric nephrology department, ankara, turkey.

background and aim: steroid-resistant nephrotic syndrome (srns) accounts for 10%-20% of all cases of idiopathic nephrotic syndrome. these patients are at risk of developing end-stage renal disease. the aim of this study was to determine the demographic characteristics, renal biopsy findings, response to immunosuppressive treatment, and prognosis in pediatric patients with srns.materials and met...

Background and Aim: Steroid-resistant nephrotic syndrome (SRNS) accounts for 10%-20% of all cases of idiopathic nephrotic syndrome. These patients are at risk of developing end-stage renal disease. The aim of this study was to determine the demographic characteristics, renal biopsy findings, response to immunosuppressive treatment, and prognosis in pediatric patients with SRNS.Materials and Met...

Thromboembolism is a rare complication of primary nephortic syndrome. Both venous and arterial thrombosis might occur in steroid responsive and steroid resistant nephrotic syndrome. This is the report of an infant with nephrotic syndrome and renovascular hypertension, complicated with asymptomatic intracardiac thrombus and managed appropriately with medical treatment.

Journal: :Clinical journal of the American Society of Nephrology : CJASN 2018
Jillian K Warejko Weizhen Tan Ankana Daga David Schapiro Jennifer A Lawson Shirlee Shril Svjetlana Lovric Shazia Ashraf Jia Rao Tobias Hermle Tilman Jobst-Schwan Eugen Widmeier Amar J Majmundar Ronen Schneider Heon Yung Gee J Magdalena Schmidt Asaf Vivante Amelie T van der Ven Hadas Ityel Jing Chen Carolin E Sadowski Stefan Kohl Werner L Pabst Makiko Nakayama Michael J G Somers Nancy M Rodig Ghaleb Daouk Michelle Baum Deborah R Stein Michael A Ferguson Avram Z Traum Neveen A Soliman Jameela A Kari Sherif El Desoky Hanan Fathy Martin Zenker Sevcan A Bakkaloglu Dominik Müller Aytul Noyan Fatih Ozaltin Melissa A Cadnapaphornchai Seema Hashmi Jeffrey Hopcian Jeffrey B Kopp Nadine Benador Detlef Bockenhauer Radovan Bogdanovic Nataša Stajić Gil Chernin Robert Ettenger Henry Fehrenbach Markus Kemper Reyner Loza Munarriz Ludmila Podracka Rainer Büscher Erkin Serdaroglu Velibor Tasic Shrikant Mane Richard P Lifton Daniela A Braun Friedhelm Hildebrandt

BACKGROUND AND OBJECTIVES Steroid-resistant nephrotic syndrome overwhelmingly progresses to ESRD. More than 30 monogenic genes have been identified to cause steroid-resistant nephrotic syndrome. We previously detected causative mutations using targeted panel sequencing in 30% of patients with steroid-resistant nephrotic syndrome. Panel sequencing has a number of limitations when compared with w...

Journal: :Genetics and molecular research : GMR 2013
J S Carrasco-Miranda R Garcia-Alvarez R R Sotelo-Mundo O Valenzuela M A Islas-Osuna N Sotelo-Cruz

Human nephrotic syndrome has been related to mutations in glomerular proteins. Mutations in the NPHS2 gene that encodes podocin have been described as responsible for steroid-resistant nephrotic syndrome. It has been advised to test for NPHS2 mutations in parallel or before giving steroid treatment in nephrotic syndrome patients in order to avoid unnecessary therapy. We identified NPHS2 mutatio...

Journal: :Genetics and molecular research : GMR 2016
Y Yang F Zhao X Tu Z Yu

Mutations in the Wilms' tumor gene, WT1, can lead to syndromic steroid-resistant nephrotic syndrome and isolated steroid-resistant nephrotic syndrome. WT1 mutations have been identified in the majority of children with Denys-Drash or Frasier syndrome. WT1 mutations have not previously been identified in boys with sporadic isolated steroid-resistant nephrotic syndrome, but, recently, four boys w...

Journal: :Indian pediatrics 2008
Ahmadzadeh Ali Derakhshan Ali Hakimzadeh Mehran Zolfigol Ali

Of 231 children with nephrotic syndrome, 87% were steroid sensitive and 13% steroid resistant. Of patients with steroid sensitive nephrotic syndrome, 38.8% were non-relapsers, 34.8% frequent relapsers and 26.4% infrequent relapsers. Among those with steroid resistant nephrotic syndrome, 37.5% had focal segmental glomerulosclerosis with a high mortality rate of 44%

Journal: :Transplantation proceedings 1991
J McCauley R Shapiro V Scantlebury N Gilboa M Jordan C Jensen A Naik A Tzakis D Ellis T E Starzl

N EPHROTIC syndrome is a broad group of disorders with diverse etiologies. In common. all have proteinuria. edema. hypercholesterolemia. and hypoalbuminemia. Steroids have proven effective in some histologic groups. but many are resistant to steroids and progress to end-stage renal disease. Transplant glomerulopathy and chronic rejection also contribute heavily to renal transplant-related nephr...

      Schimke immune-osseous dysplasia (SIOD) is a rare autosomal recessive disorder presented with specific facial features, skeletal dysplasia, steroid resistance nephrotic syndrome (SRNS) and cellular immune insufficiency. This is a SIOD case reported from Iran. He was 5 years old boy when evaluated for proteinuria and short stature. In appearance, we detected hyperpigmented macules, kyphosc...

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