Literature DB >> 9260259

Renal problems in black South African children.

P D Thomson1.   

Abstract

Black South African children have an increased prevalence of acute post-streptococcal glomerulonephritis, focal glomerulosclerosis, hepatitis B-associated membranous nephropathy, congenital syphilis, congenital nephrotic syndrome with Alport-like basement membrane changes and Takayasu's arteritis, but a paucity of reflux nephropathy, polycystic kidney disease and non-shigella-induced haemolytic uraemic syndrome. However, in recent years, the haemolytic uraemic syndrome has become more prevalent in black children; this is usually due to Shigella dysenteriae type 1, and could indicate a different emphasis in the pathogenic mechanism. Focal glomerulosclerosis is the commonest reason for renal failure requiring transplantation in black children with rapidly progressive glomerulonephritis (usually streptococcal induced) being second. Transplantation has been somewhat problematic with a scarcity of kidneys at times, many mismatches and poor compliance in the lower socio-economic groups. The association of tuberculosis with focal glomerulosclerosis and Takayasu's arteritis in black South African children is intriguing. The progression of focal glomerulosclerosis is accelerated in those patients with evidence of previous tuberculosis, and in Takayasu's arteritis the association is almost absolute as experienced locally, with the data suggesting an autoimmune reaction.

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Year:  1997        PMID: 9260259     DOI: 10.1007/s004670050330

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  8 in total

1.  Variants of alpha 1-proteinase inhibitor in black and white South African patients with focal glomerulosclerosis and minimal change nephrotic syndrome.

Authors:  A C Halkas; M C Gaillard; P D Thomson; S L Green; H Ludewick; U Kala
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

2.  Minimal change nephrotic syndrome in a patient with strongyloidiasis.

Authors:  Mieko Miyazaki; Masahito Tamura; Narutoshi Kabashima; Ryota Serino; Tatsuya Shibata; Tetsu Miyamoto; Yumi Furuno; Tetsuo Nishio; Jiro Ohara; Toshihiro Sakurai; Yutaka Otsuji
Journal:  Clin Exp Nephrol       Date:  2010-03-12       Impact factor: 2.801

3.  Oedema with proteinuria in Gambian children--a descriptive study.

Authors:  Hilary A Archer; Marianne van der Sande; Peter Hoyer; Tessa Goetghebuer; Keith P W J McAdam; Udo Vester; Melanie J Newport
Journal:  Pediatr Nephrol       Date:  2006-01-11       Impact factor: 3.714

4.  The incidence of the nephrotic syndrome in childhood in Germany.

Authors:  Ingo Franke; Malik Aydin; Corinna Elke Llamas Lopez; Lisa Kurylowicz; Rainer Ganschow; Michael Lentze; Mark Born
Journal:  Clin Exp Nephrol       Date:  2017-06-22       Impact factor: 2.801

Review 5.  Racial differences of early vascular aging in children and adolescents.

Authors:  Ruan Kruger; Lebo Francina Gafane-Matemane; Juliana Kagura
Journal:  Pediatr Nephrol       Date:  2020-05-22       Impact factor: 3.714

6.  Clinical course & management of childhood nephrotic syndrome in Germany: a large epidemiological ESPED study.

Authors:  Ingo Franke; Malik Aydin; Lisa Kurylowicz; Corinna Elke Llamas Lopez; Rainer Ganschow; Michael J Lentze; Mark Born
Journal:  BMC Nephrol       Date:  2019-02-07       Impact factor: 2.388

7.  Idiopathic nephrotic syndrome in South African children.

Authors:  Yassir Mahgoub Bakhiet; Abdullahi Mudi; Tholang Khumalo; Glenda Moonsamy; Cecil Levy
Journal:  Afr Health Sci       Date:  2017-12       Impact factor: 0.927

8.  Clinical presentation and outcome of autosomal dominant polycystic kidney disease in Nigeria.

Authors:  Fatiu A Arogundade; Akinwumi A Akinbodewa; Abefe A Sanusi; Oluyomi Okunola; Muzamil O Hassan; Adewale Akinsola
Journal:  Afr Health Sci       Date:  2018-09       Impact factor: 0.927

  8 in total

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