نتایج جستجو برای: steroid resistant nephrotic syndrome

تعداد نتایج: 842591  

Journal: :Clinical journal of the American Society of Nephrology : CJASN 2013
Hugh J McCarthy Agnieszka Bierzynska Matt Wherlock Milos Ognjanovic Larissa Kerecuk Shivaram Hegde Sally Feather Rodney D Gilbert Leah Krischock Caroline Jones Manish D Sinha Nicholas J A Webb Martin Christian Margaret M Williams Stephen Marks Ania Koziell Gavin I Welsh Moin A Saleem

BACKGROUND AND OBJECTIVES Up to 95% of children presenting with steroid-resistant nephrotic syndrome in early life will have a pathogenic single-gene mutation in 1 of 24 genes currently associated with this disease. Others may be affected by polymorphic variants. There is currently no accepted diagnostic algorithm for clinical genetic testing. The hypothesis was that the increasing reliability ...

2016
Taiwo Augustina Ladapo Christopher Imokhuede Esezobor Foluso Ebunoluwa Lesi

INTRODUCTION Children with steroid resistant nephrotic syndrome usually require treatment with second-line agents and calcineurin inhibitors such as cyclosporine are now recommended as initial therapy. These agents only recently become available in our environment and their impact on care is unknown. We reviewed the short-term treatment outcomes of their use in comparison with previous outcomes...

2016
Andrew P. Groves Patrick Reich Binayak Sigdel T. Keefe Davis

Pneumococcal-associated hemolytic uremic syndrome (pHUS) is a rare but severe complication of invasive Streptococcus pneumoniae infection. We report the case of a 12-year-old female with steroid-resistant nephrotic syndrome treated with adrenocorticotrophic hormone (H.P. Acthar(®) Gel), who developed pneumococcal pneumonia and subsequent pHUS. While nephrotic syndrome is a well-known risk facto...

Journal: :Kidney international 2004
A J Howie D Adu

2. CARIDI G, BERTELLI R, DI DUCA M, et al: Broadening the spectrum of diseases related to podocin mutations. J Am Soc Nephrol 14:1278– 1286, 2003 3. RUF RG, LICHTENBERGER A, KARLE SM, et al: Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. J Am Soc Nephrol 15:722–732, 2004 4. CARRARO M, CARIDI G, BRUSCHI M, et al: Serum glomerular pe...

2016
Rahul Chanchlani Rulan S. Parekh

Nephrotic syndrome is a common glomerular disease in children with significant variability in both incidence and steroid responsiveness among various ethnic groups. The average incidence of nephrotic syndrome is 2-16.9 per 100,000 children worldwide. Understanding the variability by ethnicity may point to potential factors leading to nephrotic syndrome, which remains elusive, and may highlight ...

Journal: :iranian journal of medical sciences 0
m. basiratnia m.h. fallahzadeh a. derakhshan g. hosseini-al-hashemi

abstract background: given the high relapse rate of disease in children with steroid dependent nephrotic syndrome and the osteoporotic effect of long periods of steroid therapy, this survey was performed to find the bone mineral status of these patients.   methods: bone mineral density and content (bmd and bmc) were measured using dual energy x-ray absorptiometry in 37 nephrotic children, six g...

2017
Noureddin Nourbakhsh Robert H Mak

Patients with steroid-resistant nephrotic syndrome (SRNS) represent a challenging subset of patients with nephrotic syndrome who often fail standard immunosuppression and have a higher likelihood of progressing to end-stage renal disease. Appropriate treatment of SRNS requires an adequate understanding of the historical treatment, renal histopathology, and genetics associated with the disease. ...

Journal: :Maedica 2010
Florentina Cucer Ingrith Miron Robert Müller Codruta Iliescu Halitchi Doina Mihaila

The management of patients with steroid-resistant nephrotic syndrome remains difficult. We repport our experience with Cyclophosphamide therapy, in an attempt to compare the results between an oral protocol and two i.v. protocols. The complete and sustained general remission rate was 43.1%, which confirms the efficacy of the treatment, especially for children with minimal change nephrotic syndr...

Alireza Baradaran-Heravi Bita Geramizadeh, Majid Yavarian Mehran Karimi, Mitra Basiratnia,

Schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphy-seal dysplasia. Mutations in SWI/SNF2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 (SMARCAL1) gene are responsible for the disease. The present report describes, for the f...

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