Cutaneous telangiectasias, sparse hair, and type I membranoproliferative glomerulonephritis

被引：0

作者：

I. R. Gupta

C. H. Tsai

J. Siegel-Bartelt

P. Thorner

J. W. Balfe

机构：

[1] Division of Nephrology,

[2] Montreal Children’s Hospital,undefined

[3] 2300 Tupper Street,undefined

[4] Montreal,undefined

[5] Quebec H3H 1P3,undefined

[6] Canada,undefined

[7] Division of Clinical Genetics,undefined

[8] University of Toronto,undefined

[9] The Hospital for Sick Children,undefined

[10] 555 University Avenue,undefined

[11] Toronto,undefined

[12] Ontario M5G 1X8,undefined

[13] Canada,undefined

[14] Division of Pathology,undefined

[15] University of Toronto,undefined

[16] The Hospital for Sick Children,undefined

[17] 555 University Avenue,undefined

[18] Toronto,undefined

[19] Ontario M5G 1X8,undefined

[20] Canada,undefined

[21] Division of Nephrology,undefined

[22] University of Toronto,undefined

[23] The Hospital for Sick Children,undefined

[24] 555 University Avenue,undefined

[25] Toronto,undefined

[26] Ontario M5G 1X8,undefined

[27] Canada,undefined

来源：

Pediatric Nephrology | 1999年 / 13卷

关键词：

Key words Membranoproliferative glomerulonephritis; Cutaneous telangiectasias; Sparse hair; Atrial septal defect; Ectodermal dysplasia;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

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.

引用

页码：129 / 131

页数：2