Keratitis, ichthyosis, deafness (KID) syndrome-the first report from India
- 1 July 1993
- journal article
- case report
- Published by Oxford University Press (OUP) in Clinical and Experimental Dermatology
- Vol. 18 (4), 386-388
- https://doi.org/10.1111/j.1365-2230.1993.tb02227.x
Abstract
A patient with the keratitis, ichthyosis and deafness (KID) syndrome is described. The patient had recurrent skin infections which led to complete scalp hair loss. The nails were dystrophic. Physical development was normal; however, his intelligence was subnormal. The erythrokeratodermatous plaques over the face, trunk and extremities were characteristic and the skin in general was dry and hyperkeratotic. Palms and soles showed marked thickening with a stippled appearance.Keywords
This publication has 6 references indexed in Scilit:
- Keratitis, Ichthyosis, and Deafness (KID) Syndrome with Adult Onset of Keratitis ComponentInternational Journal of Dermatology, 1990
- Corneal effect of isotretinoin: Possible exacerbation of corneal neovascularization in a patient with the keratitis, ichthyosis, deafness (“KID”) syndromeJournal of the American Academy of Dermatology, 1986
- KID Syndrome (Keratitis, Ichthyosis, and Deafness) and Chronic Mucocutaneous Candidiasis: Case Report and Review of the LiteraturePediatric Dermatology, 1984
- The keratitis, ichthyosis, and deafness (KID) syndromeArchives of Dermatology, 1981
- Atypical ichthyosiform erythroderma, deafness and keratitis.British Journal of Dermatology, 1976
- Generalized spiny hyperkeratosis, universal alopecia, and deafness. A previously undescribed syndromeArchives of Dermatology, 1969