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A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy

Many types of inherited renal diseases have ocular features that occasionally support a diagnosis. The following study describes an unusual example of a 40-year-old woman with granular corneal dystrophy type II complicated by renal involvement. These two conditions may coincidentally coexist; howeve...

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Detalles Bibliográficos
Autores principales: Iwafuchi, Yoichi, Morioka, Tetsuo, Oyama, Yuko, Nozu, Kandai, Iijima, Kazumoto, Narita, Ichiei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073658/
https://www.ncbi.nlm.nih.gov/pubmed/27781206
http://dx.doi.org/10.1159/000449129