Multicystic Dysplastic Kidney in Association With Congenital Ichthyosiform Erythroderma

Authors

  • Hamid Reza Badeli Division of Nephrology, Department of Pediatrics, Guilan University of Medical Sciences, Rasht, Iran Author
  • Seyed Aidin Sajedi Division of Nephrology, Department of Pediatrics, Guilan University of Medical Sciences, Rasht, Iran Author
  • Azita Tangestaninejad Department of Internal Medicine, Guilan University of Medical Sciences, Rasht, Iran Author
  • Mohammad Reza Ahmadian Division of Nephrology, Department of Pediatrics, Guilan University of Medical Sciences, Rasht, Iran Author
  • Kaveh Alipour Kanafi Division of Nephrology, Department of Pediatrics, Guilan University of Medical Sciences, Rasht, Iran Author

Abstract

Multicystic dysplastic kidney is a noninherited congenital disease. Association of this disease with abnormalities of various organs is common. We, however, report a rare case of multicystic dysplastic kidney associated with congenital ichthyosiform erythroderma in an infant. Different developmental origins of the skin and the kidney can explain the scarcity of concurrent congenital skin and kidney abnormalities. Nonetheless, the development of both organs depends on mesenchyme-epithelial interactions for inductive signaling. It seems defects in the production of signaling molecules can explain such an association.

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Published

2009-04-11

Issue

Section

CASE REPORT | Kidney Diseases

How to Cite

Multicystic Dysplastic Kidney in Association With Congenital Ichthyosiform Erythroderma. (2009). Iranian Journal of Kidney Diseases, 1(2), 102-104. https://www.ijkd.org/index.php/ijkd/article/view/53