| Literature DB >> 18319008 |
Ali Abdollahi1, Zahra Hallaji, Nafiseh Esmaili, Mahin Valikhani, Masoumeh Barzegari, Maryam Akhyani, Siavash Toosi, Alireza Miresmaili.
Abstract
KID syndrome is a rare congenital disorder characterized by keratitis, ichthyosis, and deafness. We have described a 4-year-old girl who is treated with bland emollients and topical keratolytics such as urea and surprisingly observed marked improvement in skin hyperkeratosis and palmoplantar keratoderma. We think that along with urgent ophthalmologic and otolaryngologic measures, simple topical therapies may improve skin condition in KID syndrome precluding the possible hazards of systemic retinoid therapy.Entities:
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Year: 2007 PMID: 18319008
Source DB: PubMed Journal: Dermatol Online J ISSN: 1087-2108