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 language | English (US) |
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Pages (from-to) | 129-131 |
Number of pages | 3 |
Journal | Pediatric Nephrology |
Volume | 13 |
Issue number | 2 |
DOIs | |
State | Published - Feb 1999 |
Keywords
- Atrial septal defect
- Cutaneous telangiectasias
- Ectodermal dysplasia
- Membranoproliferative glomerulonephritis
- Sparse hair
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Nephrology