Literature DB >> 626446

Hereditary nephritis: a re-examination of its clinical and genetic features.

W M O'Neill, C L Atkin, H A Bloomer.   

Abstract

In order to re-evaluate current concepts of hereditary nephritis we studied the urinary findings, the course of the disease, and its genetic transmission in two large pedigrees. We identified 150 patients with hereditary nephritis. Our data show that microscopic hematuria is the most reliable urinary criterion for diagnosing hereditary nephritis in both male and female patients. The hematuria is frequently accompanied by erythrocyte casts indicating that the renal lesion is a glomerulitis. Men are more severely affected than women. They have striking urinary abnormalities, which are present in early childhood, and they progress to renal failure in adult life. Affected women have less obvious urinary abnormalities and rarely develop uremia. In these two families a sex-linked dominant mode of genetic transmission was present. The demonstration that hereditary nephritis is X-linked, at least in some families, helps to explain the difference in severity between men and women and the variable expression among affected women.

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Year:  1978        PMID: 626446     DOI: 10.7326/0003-4819-88-2-176

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  17 in total

Review 1.  Alport syndrome, basement membranes and collagen.

Authors:  C E Kashtan; M M Kleppel; R J Butkowski; A F Michael; A J Fish
Journal:  Pediatr Nephrol       Date:  1990-09       Impact factor: 3.714

2.  A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.

Authors:  D F Barker; C J Pruchno; X Jiang; C L Atkin; E M Stone; J C Denison; P R Fain; M C Gregory
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

Review 3.  Alport's syndrome.

Authors:  M A Crawfurd
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

4.  Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis.

Authors:  C Kashtan; A J Fish; M Kleppel; K Yoshioka; A F Michael
Journal:  J Clin Invest       Date:  1986-10       Impact factor: 14.808

5.  A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.

Authors:  B D Edwards; M A Patton; S A Dilly; J B Eastwood
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

6.  The NC1 domain of collagen type IV in neonatal dog glomerular basement membranes. Significance in Samoyed hereditary glomerulopathy.

Authors:  P Thorner; R Baumal; A Binnington; V E Valli; P Marrano; H Clarke
Journal:  Am J Pathol       Date:  1989-05       Impact factor: 4.307

Review 7.  Genetics of Alport's syndrome.

Authors:  J Feingold; E Bois
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

8.  Samoyed hereditary glomerulopathy (SHG). Evolution of splitting of glomerular capillary basement membranes.

Authors:  B Jansen; P Thorner; R Baumal; V Valli; M G Maxie; A Singh
Journal:  Am J Pathol       Date:  1986-12       Impact factor: 4.307

9.  Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?

Authors:  J A Govan
Journal:  Br J Ophthalmol       Date:  1983-08       Impact factor: 4.638

10.  Samoyed hereditary glomerulopathy: serial, clinical and laboratory (urine, serum biochemistry and hematology) studies.

Authors:  B Jansen; V E Valli; P Thorner; R Baumal; J H Lumsden
Journal:  Can J Vet Res       Date:  1987-07       Impact factor: 1.310

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