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Published on: August 20, 2019
Rare Association of Waardenburg Syndrome with Minimal Change Disease
G Anvesh1, S B Raju1, K Prasad1
1Department of Nephrology, Nizam's Institute of Medical Sciences, Hyderabad, Telangana, India.
Abstract:
Waardenburg syndrome (WS) is a rare genetic disorder characterized by varying degrees of hearing loss, pigmentary anomalies, and defects of other neural crest cell-derived structures. The association of WS with renal anomalies has been described in the literature. However, nephrotic syndrome is a very rare association with WS, and only one case has been reported in the literature. We report a case of WS2 associated with biopsy-proven nephrotic syndrome (minimal change disease).
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