Dominantly inherited glomerulonephritis and an unusual skin disease.

Author:

Sherwood M C,Pincott J R,Goodwin F J,Dillon M J

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference4 articles.

1. Chromosomal breakage and acute leukaemia in congenital telangiectasia erythema and stunted growth;Sawitsky, A.; Bloom, D.; German, J.;Ann Intern Med,1966

2. Renal lesions in Cockayne's syndrome;Ohno, T.; Hirooka, M.;Tohoku J Exp Med; specimens in these patients showed hyalinisation of glomeruli, tubular atrophy, and interstitial fibrosis.3 The other typical clinical features of these conditions were not apparent in the patient or his father,1966

3. Familial Clq deficiency in 3 siblings with glomerulonephritis and Rothmund-Thomson syndrome;Mampaso, F.; Ecija, J.; Fogue, L.; Moneo, I.; Gallego, N.; LeyvaCobian, F.;Nephron,1981

4. X-linked mesangiocapillary glomerulonephritis;Stutchfield, P.R.; White, R.H.R.; Cameron, A.H.; Thompson, R.A.; Mackintosh, P.; Wells, L.;Clin Nephrol,1986

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