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Cutaneous telangiectasias, sparse hair, and type I membranoproliferative glomerulonephritis |
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| Authors: | I. R. Gupta C. H. Tsai J. Siegel-Bartelt P. Thorner J. W. Balfe |
| Affiliation: | (1) Division of Nephrology, Montreal Children’s Hospital, 2300 Tupper Street, Montreal, Quebec H3H 1P3, Canada, CA;(2) Division of Clinical Genetics, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada, CA;(3) Division of Pathology, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada, CA;(4) Division of Nephrology, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada, CA |
| 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. Received: 29 December 1997 / Revised: 6 May 1998 / Accepted: 21 May 1998 |
| Keywords: | Membranoproliferative glomerulonephritis Cutaneous telangiectasias Sparse hair Atrial septal defect Ectodermal dysplasia |
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