Literature DB >> 3153309

Alport's syndrome as a cause of renal failure in Europe.

N Gretz1, M Broyer, F P Brunner, H Brynger, R A Donckerwolcke, C Jacobs, P Kramer, N H Selwood, A J Wing.   

Abstract

We studied the geographical distribution, male to female ratio, and age at the start of renal replacement therapy (RRT) for end-stage renal failure (ESRF) in 600 patients with hereditary nephritis with nerve deafness (Alport's syndrome) reported to the European Dialysis and Transplant Association Registry since 1975. Annual age- and sex-specific acceptance rates for RRT showed a variable peak incidence according to country, ranging between, 0 and 2.4 patients per million population in males aged 15-24 years, but with only about half this incidence in females. In Scandinavian countries there were very few females who started RRT, and males were older than in the rest of Europe. The overall male to female ratio was 4:1. The median age at the start of RRT was: males (n = 479) 24.3 years (1st quartile 19.5 years; 3rd quartile 31.5 years); females (n = 121) 31.5 years (1st quartile 23.0 years; 3rd quartile 43.2 years). Our study provided confirmation that males reach ESRF earlier than females. In addition, we detected previously unrecognized geographical differences.

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Year:  1987        PMID: 3153309     DOI: 10.1007/bf00849245

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


  11 in total

Review 1.  FAMILIAL ASPECTS OF DIFFUSE RENAL DISEASES.

Authors:  G T PERKOFF
Journal:  Annu Rev Med       Date:  1964       Impact factor: 13.739

2.  The genetics of the Alport syndrome.

Authors:  P V Tishler; B Rosner
Journal:  Birth Defects Orig Artic Ser       Date:  1974

3.  Progressive and nonprogressive hereditary chronic nephritis.

Authors:  J P Grünfeld; E P Bois; N Hinglais
Journal:  Kidney Int       Date:  1973-09       Impact factor: 10.612

4.  Hereditary nephritis. Clinical spectrum and mode of inheritance in five new kindreds.

Authors:  J A Chazan; J Zacks; J J Cohen; S Garella
Journal:  Am J Med       Date:  1971-06       Impact factor: 4.965

5.  Familial nephritis associated with the nephrotic syndrome. In a family with severe involvement in females.

Authors:  M S Albert; J M Leeming; H J Wigger
Journal:  Am J Dis Child       Date:  1969-02

6.  Combined Report on Regular Dialysis and Transplantation in Europe, IX, 1978.

Authors:  F P Brunner; H Brynger; C Chantler; R A Donckerwolcke; R A Hathway; C Jacobs; N H Selwood; A J Wing
Journal:  Proc Eur Dial Transplant Assoc       Date:  1979

7.  Alport's syndrome. A report of 58 cases and a review of the literature.

Authors:  M Gubler; M Levy; M Broyer; C Naizot; G Gonzales; D Perrin; R Habib
Journal:  Am J Med       Date:  1981-03       Impact factor: 4.965

8.  Familial hereditary nephropathy (Alport's syndrome).

Authors:  P Purriel; M Drets; E Pascale; R Sánchez Cestau; A Borrás; W A Ferreira; A de Lucca; L Fernández
Journal:  Am J Med       Date:  1970-12       Impact factor: 4.965

9.  Juvenile nephronophthisis and medullary cystic disease--the same disease (report of a large family with medullary cystic disease associated with gout and epilepsy).

Authors:  J R Burke; J A Inglis; P W Craswell; K R Mitchell; B T Emmerson
Journal:  Clin Nephrol       Date:  1982-07       Impact factor: 0.975

10.  Chronic hereditary nephritis. A clinicopathologic study of 23 new kindreds and review of the literature.

Authors:  G H Farboody; R Valenzuela; L J McCormack; R Kallen; D G Osborne
Journal:  Hum Pathol       Date:  1979-11       Impact factor: 3.466

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  4 in total

1.  Improving mutation screening in familial hematuric nephropathies through next generation sequencing.

Authors:  Vincent Morinière; Karin Dahan; Pascale Hilbert; Marieline Lison; Said Lebbah; Alexandra Topa; Christine Bole-Feysot; Solenn Pruvost; Patrick Nitschke; Emmanuelle Plaisier; Bertrand Knebelmann; Marie-Alice Macher; Laure-Hélène Noel; Marie-Claire Gubler; Corinne Antignac; Laurence Heidet
Journal:  J Am Soc Nephrol       Date:  2014-05-22       Impact factor: 10.121

2.  The paediatric registry of the European Dialysis and Transplant Association: 20 years' experience.

Authors:  M Broyer; C Chantler; R Donckerwolcke; J H Ehrich; G Rizzoni; K Schärer
Journal:  Pediatr Nephrol       Date:  1993-12       Impact factor: 3.714

3.  An electrophysiological study on children and young adults with Alport's syndrome.

Authors:  B G Jeffrey; M Jacobs; G Sa; T M Barratt; D Taylor; A Kriss
Journal:  Br J Ophthalmol       Date:  1994-01       Impact factor: 4.638

4.  Phenotype variability in a large Spanish family with Alport syndrome associated with novel mutations in COL4A3 gene.

Authors:  C Cervera-Acedo; A Coloma; E Huarte-Loza; M Sierra-Carpio; E Domínguez-Garrido
Journal:  BMC Nephrol       Date:  2017-10-31       Impact factor: 2.388

  4 in total

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