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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:	Case Report
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

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