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Incidence of pediatric glomerular diseases in Arab world: A systematic review.
Saudi J Kidney Dis Transpl
May 2020
Department of Allied Health Sciences, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Sultanate of Oman.
Despite the high number of Arab children, there are a scanty available data about different types of pediatric glomerular diseases in all Arab countries. Very few Arab countries have a national renal biopsy registry. In this review, we performed a systematic review analyzing the incidence of pediatric glomerular disease in all Arab countries.
View Article and Find Full Text PDFChildhood idiopathic steroid-resistant nephrotic syndrome at a Single Center in Khartoum.
Saudi J Kidney Dis Transpl
July 2019
Department of Pediatrics, Pediatric Nephrology Unit, Soba University Hospital, Khartoum, Sudan.
Prevalence, clinicopathological features, and outcome of childhood idiopathic steroid-resistant nephrotic syndrome (ISRNS) vary in different countries. We report on these parameters in a single center in Khartoum. We retrospectively reviewed all the records of children with idiopathic nephrotic syndrome (INS) followed up in the pediatric renal unit, Soba Hospital, Khartoum between 2001 and 2012.
View Article and Find Full Text PDFFamilial partial lipodystrophy and proteinuric renal disease due to a missense c.1045C > T mutation.
Endocrinol Diabetes Metab Case Rep
June 2017
Departments of Endocrinology.
Unlabelled: Proteinuric renal disease is prevalent in congenital or acquired forms of generalized lipodystrophy. In contrast, an association between familial partial lipodystrophy (FPLD) and renal disease has been documented in very few cases. A 22-year-old female patient presented with impaired glucose tolerance, hyperinsulinemia, hirsutism and oligomenorrhea.
View Article and Find Full Text PDFChildhood Idiopathic Steroid Resistant Nephrotic Syndrome, Different Drugs And Outcome.
J Ayub Med Coll Abbottabad
December 2017
Department of Paediatric Nephrology, the Children's Hospital and the Institute of Child Health, Lahore, Pakistan.
Background: The management of steroid resistant nephrotic syndrome (SRNS) is quite difficult in paediatric patients. Not only the remission is difficult but also these patients are at risk of progression to end stage renal disease (ESRD). The goal of treatment is either to achieve complete remission or even partial remission as it is the most important predictor of disease outcome.
View Article and Find Full Text PDFEarly Markers of Tubulointerstitial Fibrosis in Children With Idiopathic Nephrotic Syndrome: Preliminary Report.
Medicine (Baltimore)
October 2015
From the Department of Pediatric Nephrology, Medical University of Lublin (BB, MZ, HB, PS, AWP); and Department of Paediatric Endocrinology and Diabetology with Endocrine-Metabolic Laboratory, Lublin, Poland (BW).
Unlabelled: Tubulointerstitial fibrosis and tubular atrophy play a crucial role in the pathogenesis of chronic kidney disease (CKD). They are also major determinants in chronic kidney disease development and progression in patients with primary renal diseases characterized by persistent or recurrent proteinuria. The purpose of the study was to assess urinary excretion of alpha-glutathione S-transferase (alpha-GST), pi-glutathione S-transferase (pi-GST), neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), and serum NGAL level in children with idiopathic nephrotic syndrome (INS).
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