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.
- Atrial septal defect
- Cutaneous telangiectasias
- Ectodermal dysplasia
- Membranoproliferative glomerulonephritis
- Sparse hair
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health