Literature DB >> 2484451

Cutaneous telangiectasia, sparse hair and membranoproliferative glomerulonephritis. A new case of a newly recognized entity.

W Proesmans1, E Legius, K Van Herck, B Van Damme.   

Abstract

A boy with sparse red hair, absent eyebrows and eyelashes, cutaneous telangiectasia, poorly developed subcutaneous fat and normocomplementaemic membranoproliferative glomerulonephritis is described. Additional findings were an old-looking, peculiar face, mild developmental delay, calcified choroid plexus and renal arteriolosclerosis. It is believed that this is a new case of a newly recognized entity.

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Year:  1989        PMID: 2484451     DOI: 10.1007/bf00852899

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


  3 in total

1.  Partial lipodystrophy and hypocomplementaemic nephritis.

Authors:  R A Thompson; R H White
Journal:  Lancet       Date:  1973-09-22       Impact factor: 79.321

2.  Dominantly inherited glomerulonephritis and an unusual skin disease.

Authors:  M C Sherwood; J R Pincott; F J Goodwin; M J Dillon
Journal:  Arch Dis Child       Date:  1987-12       Impact factor: 3.791

3.  Familial C1q deficiency in 3 siblings with glomerulonephritis and Rothmund-Thomson syndrome.

Authors:  F Mampaso; J Ecija; L Fogue; I Moneo; N Gallego; F Leyva-Cobian
Journal:  Nephron       Date:  1981       Impact factor: 2.847

  3 in total

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