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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Detalles Bibliográficos
Autores principales: Anvesh, G., Raju, S. B., Prasad, K., Sharma, A., Surendra, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998718/
https://www.ncbi.nlm.nih.gov/pubmed/29962674
http://dx.doi.org/10.4103/ijn.IJN_55_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998718/
https://www.ncbi.nlm.nih.gov/pubmed/29962674
http://dx.doi.org/10.4103/ijn.IJN_55_17

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