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Rare Association of Waardenburg Syndrome with Minimal Change Disease
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 ve...
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| Publicado no: | Indian J Nephrol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5998718/ https://ncbi.nlm.nih.gov/pubmed/29962674 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijn.IJN_55_17 |
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