KID syndrome

A rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss.

Palmoplantar hyperkeratosis

Hyperkeratosis affecting the palm of the hand and the sole of the foot.


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(per page)
PMID (PMCID)
24741331
(3970942)
 OTHER
Keratitis-ichthyosis-deafness syndrome: first affected family reported in the Middle East.
Al Fahaad H.
Int Med Case Rep J. 2014;7:63-6.
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.