Cutaneous telangiectasias, sparse hair, and type I membranoproliferative glomerulonephritis

I. R. Gupta, C. H. Tsai, J. Siegel-Bartelt, P. Thorner, J. W. Balfe

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

We report the unusual association of normocomplementemic type I membranoproliferative glomerulonephritis in a 10-year-old girl with sparse red hair, absent eyebrows and eyelashes, cutaneous telangiectasias, and an atrial septal defect.

Original languageEnglish (US)
Pages (from-to)129-131
Number of pages3
JournalPediatric Nephrology
Volume13
Issue number2
DOIs
StatePublished - Feb 1 1999

Keywords

  • Atrial septal defect
  • Cutaneous telangiectasias
  • Ectodermal dysplasia
  • Membranoproliferative glomerulonephritis
  • Sparse hair

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Nephrology

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    Gupta, I. R., Tsai, C. H., Siegel-Bartelt, J., Thorner, P., & Balfe, J. W. (1999). Cutaneous telangiectasias, sparse hair, and type I membranoproliferative glomerulonephritis. Pediatric Nephrology, 13(2), 129-131. https://doi.org/10.1007/s004670050578