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Literature DB >> 7742208

Inherited factor H deficiency and collagen type III glomerulopathy.

B A Vogt¹, R J Wyatt, B A Burke, S C Simonton, C E Kashtan.

Abstract

A non-immune complex-mediated glomerulonephritis associated with persistent hypocomplementemia occurred in a young boy. Measurement of complement components revealed complete factor H deficiency, inherited as an autosomal recessive trait. Evaluation of the renal lesion revealed extensive deposition of type III collagen suggestive of collagen type III glomerulopathy, a recently identified cause of chronic renal insufficiency in children and adults. This report represents the first association of inherited factor H deficiency with collagen type III glomerulopathy.

Entities: Disease Gene Mutation Species

Mesh：

Substances：

Year: 1995 PMID： 7742208 DOI： 10.1007/BF00858956

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

15 in total

1. Combined homozygous factor H and heterozygous C2 deficiency in an Italian family.

Authors: M Brai; G Misiano; S Maringhini; I Cutaja; G Hauptmann
Journal: J Clin Immunol Date: 1988-01 Impact factor: 8.317

2. A case of collagenofibrotic glomerulopathy associated with hepatic perisinusoidal fibrosis.

Authors: S Mizuiri; A Hasegawa; A Kikuchi; Y Amagasaki; N Nakamura; H Sakaguchi
Journal: Nephron Date: 1993 Impact factor: 2.847

3. Glomerular localization of type III collagen in human kidney disease.

Authors: K Yoshioka; T Takemura; M Tohda; N Akano; H Miyamoto; A Ooshima; S Maki
Journal: Kidney Int Date: 1989-05 Impact factor: 10.612

4. Hereditary, complete deficiency of complement factor H associated with recurrent meningococcal disease.

Authors: H E Nielsen; K C Christensen; C Koch; B S Thomsen; N H Heegaard; J Tranum-Jensen
Journal: Scand J Immunol Date: 1989-12 Impact factor: 3.487

5. Primary glomerular fibrosis: a new nephropathy caused by diffuse intra-glomerular increase in atypical type III collagen fibers.

Authors: K Ikeda; H Yokoyama; N Tomosugi; H Kida; A Ooshima; K Kobayashi
Journal: Clin Nephrol Date: 1990-04 Impact factor: 0.975

6. Immunofluorescence studies of dense deposit disease. The presence of railroad tracks and mesangial rings.

Authors: Y Kim; R L Vernier; A J Fish; A F Michael
Journal: Lab Invest Date: 1979-04 Impact factor: 5.662

7. Collagen type III glomerulopathy: a new type of hereditary nephropathy.

Authors: M C Gubler; J P Dommergues; M Foulard; A Bensman; J P Leroy; M Broyer; R Habib
Journal: Pediatr Nephrol Date: 1993-08 Impact factor: 3.714

Review 8. Collagen type III glomerulopathy: a new idiopathic glomerular disease.

Authors: E Imbasciati; G Gherardi; K Morozumi; F Gudat; R Epper; V Basler; M J Mihatsch
Journal: Am J Nephrol Date: 1991 Impact factor: 3.754

9. H deficiency in two brothers with atypical dense intramembranous deposit disease.

Authors: M Levy; L Halbwachs-Mecarelli; M C Gubler; G Kohout; A Bensenouci; P Niaudet; G Hauptmann; P Lesavre
Journal: Kidney Int Date: 1986-12 Impact factor: 10.612

10. ISOLATION OF BETA IF-GLOBULIN FROM HUMAN SERUM AND ITS CHARACTERIZATION AS THE FIFTH COMPONENT OF COMPLEMENT.

Authors: U R NILSSON; H J MUELLER-EBERHARD
Journal: J Exp Med Date: 1965-08-01 Impact factor: 14.307

16 in total

1. The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion.

Authors: Guido A Hegasy; Tamara Manuelian; Kolbjorn Hogasen; Johan H Jansen; Peter F Zipfel
Journal: Am J Pathol Date: 2002-12 Impact factor: 4.307

Review 2. C3 Glomerulopathy.

Authors: Magdalena Riedl; Paul Thorner; Christoph Licht
Journal: Pediatr Nephrol Date: 2016-04-07 Impact factor: 3.714

3. Two brothers with collagenofibrotic glomerulopathy.

Authors: Takafumi Aoki; Kazuyuki Hayashi; Takatoshi Morinaga; Hidetaka Tomida; Manabu Hishida; Satoko Yamamoto; Nobuyuki Kajiwara; Hirofumi Tamai
Journal: CEN Case Rep Date: 2014-09-18

4. Glomerulopathy with distinctive fibrillar deposits but lacking glomerular deposition of type III collagen.

Authors: Tatsuo Yamamoto; Akashi Togawa; Masanobu Eguchi; Naro Ohashi; Hideo Yasuda; Yutaka Harita; Motoshi Hattori; Yutaka Yamaguchi; Kunio Ohyama
Journal: CEN Case Rep Date: 2016-03-08

5. Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.

Authors: L Ying; Y Katz; M Schlesinger; R Carmi; H Shalev; N Haider; G Beck; V C Sheffield; D Landau
Journal: Am J Hum Genet Date: 1999-12 Impact factor: 11.025

Review 6. Dense deposit disease.

Authors: Richard J H Smith; Claire L Harris; Matthew C Pickering
Journal: Mol Immunol Date: 2011-05-24 Impact factor: 4.407

Review 10. Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.

Authors: M C Pickering; H T Cook
Journal: Clin Exp Immunol Date: 2008-02 Impact factor: 4.330