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Cutaneous telangiectasias, sparse hair, and type I membranoproliferative glomerulonephritis

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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.

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Authors and Affiliations

  1. Division of Nephrology, Montreal Children’s Hospital, 2300 Tupper Street, Montreal, Quebec H3H 1P3, Canada, , , , , , CA

    I. R. Gupta

  2. Division of Clinical Genetics, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada, , , , , , CA

    C. H. Tsai & J. Siegel-Bartelt

  3. Division of Pathology, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada, , , , , , CA

    P. Thorner

  4. Division of Nephrology, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada, , , , , , CA

    J. W. Balfe

Authors
  1. I. R. Gupta
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  2. C. H. Tsai
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  3. J. Siegel-Bartelt
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  4. P. Thorner
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  5. J. W. Balfe
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Received: 29 December 1997 / Revised: 6 May 1998 / Accepted: 21 May 1998

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Gupta, I., Tsai, C., Siegel-Bartelt, J. et al. Cutaneous telangiectasias, sparse hair, and type I membranoproliferative glomerulonephritis. Pediatr Nephrol 13, 129–131 (1999). https://doi.org/10.1007/s004670050578

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  • DOI: https://doi.org/10.1007/s004670050578

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