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Keratitis–ichthyosis–deafness syndrome: first affected family reported in the Middle East
INTRODUCTION: Keratitis–ichthyosis–deafness (KID) syndrome is a rare congenital multisystem disorder affecting certain tissues of ectodermal origin such as epidermis, cochlea, and cornea, leading mainly to palmoplantar hyperkeratosis, ichthyosiform scaling, deafness, and blindness. The author report...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970942/ https://www.ncbi.nlm.nih.gov/pubmed/24741331 http://dx.doi.org/10.2147/IMCRJ.S58432 |