Results 21 to 30 of about 60,277 (228)

Congenital nephrotic syndrome

Srpski arhiv za celokupno lekarstvo, 2008
INTRODUCTION. Congenital nephrotic syndrome is usually presented with heavy proteinuria, hypoproteinaemia, oedema and hyperlipidaemia in a child from its birth until the age of 3 months. Aetiology of the disease is mutation in the relevant gene or it develops secondary to various infections.
Natasa, Stajić, Jovana, Putnik, Aleksandra, Paripović, Slavisa, Djurić, Radovan, Bogdanović   +4 more
openaire   +2 more sources

Outcome of participants with nephrotic syndrome in combined clinical trials of lupus nephritis

Lupus Science and Medicine, 2019
Objective The outcome of participants with nephrotic syndrome in clinical trials of lupus nephritis has not been studied in detail.Methods Collated data from two randomised controlled trials in lupus nephritis, Lupus Nephritis Assessment of Rituximab ...
Brad Rovin, Maria Dall’Era, Paul Brunetta, Liliana Michelle Gomez Mendez, Matthew D Cascino, Tamiko R Katsumoto, Paul Brakeman, Jay Garg   +7 more
doaj   +1 more source

A rare presentation of type II Abernethy malformation and nephrotic syndrome: Case report and review

Open Life Sciences, 2022
Type II Abernethy malformation is an extremely reported congenital extrahepatic portosystemic shunt in complication with nephrotic syndrome. We present the case of an 8-year-old boy who presented with symptoms of type II Abernethy malformation and ...
Wu Xin, Gu Weizhong, Lin Yongzhi, Ye Lina   +3 more
doaj   +1 more source

Nephrotic syndrome redux [PDF]

Nephrology Dialysis Transplantation, 2014
Redux: brought back, resurgent (Wikipedia free dictionary). This essay traces the history of the concepts that led to the usage of the term 'nephrotic syndrome' beginning ∼90 years ago. We then examined the various definitions used for this syndrome and modified them to conform to contemporary standards.
Richard J, Glassock, Fernando C, Fervenza, Lee, Hebert, J Stewart, Cameron   +3 more
openaire   +2 more sources

Klippel–Trenaunay–Weber syndrome with atypical presentation of hypersplenism and nephrotic syndrome: a case report

Journal of Medical Case Reports, 2017
Background Klippel–Trenaunay–Weber syndrome is a rare syndrome; unfortunately, very few studies of the connection between hypersplenism, nephrotic syndrome, and Klippel–Trenaunay–Weber syndrome have been published. Case presentation We report the case of
Linda Kundzina, Sandra Lejniece
doaj   +1 more source

Spontaneous remission of nephrotic syndrome associated with COVID-19 infection in an 8-year-old boy

The Turkish Journal of Pediatrics, 2022
Background. It is already known that viral infections, exclusively upper respiratory tract infections may trigger relapses of nephrotic syndrome. Recently, COVID-19 disease has also been reported to be related with relapse of nephrotic syndrome in
Aylin Kayalı Akyol, Gamze Akça Dinç, Özlem Mustafaoğlu, Aysun Yahşi, Gülsüm İclal Bayhan, Sare Gülfem Özlü   +5 more
doaj   +1 more source

A Case of Dasatinib Induced Nephrotic Syndrome in a Chronic Myeloid Leukemia Patient with Steroid Dependent Nephrotic Syndrome

Clinical Pediatric Hematology-Oncology
Tyrosine kinase (TK) inhibitors are most common used to treat chronic myeloid leukemia (CML). Several studies describe a range of adverse effects of TK inhibitors on the kidney in adult patients, including nephrotic syndrome.
Jeongjin Lee, Nack-Gyun Chung, Yeong Jin Choi, Yeonhee Lee   +3 more
doaj   +1 more source

Monogenic Causes of Proteinuria in Children

Frontiers in Medicine, 2018
Glomerular disease is a common cause for proteinuria and chronic kidney disease leading to end-stage renal disease requiring dialysis or kidney transplantation in children.
Onur Cil, Farzana Perwad
doaj   +1 more source

Anti-Rituximab Antibodies Occurrence and Clinical Outcomes in Patients With Primary Membranous Nephropathy

Kidney International Reports
Introduction: Rituximab is a first-line treatment for primary membranous nephropathy (pMN), with proven efficacy and safety. The use of monoclonal antibodies such as rituximab can lead to the formation of antidrug antibodies that may interfere with the ...
Marco Allinovi, Maxime Teisseyre, Matteo Accinno, Cecilia Finocchi, Vincent L.M. Esnault, Marion Cremoni, Tommaso Mazzierli, Daniela Lazzarini, Micaela Anna Casiraghi, Céline Fernandez, Kévin Zorzi, Vesna Brglez, Lorenzo Cosmi, Andrea Matucci, Leonardo Caroti, Giulia Antognoli, Calogero Lino Cirami, Alessandra Vultaggio, Barbara Seitz-Polski   +18 more
doaj   +1 more source

Emerging Role of SH3BP2 as Regulator of Immune and Nonimmune Cells in Nephrotic Syndrome

Glomerular Diseases
Background: Minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) are major forms of nephrotic syndrome that remain difficult to treat. MCD and FSGS have distinct but also overlapping clinical, histological, metabolic, and
Tarak Srivastava, Mukut Sharma
doaj   +1 more source