| Keratitis-ichthyosis-deafness syndrome |
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| Other names |
"Erythrokeratodermia progressiva Burns", "Ichthyosiform erythroderma, corneal involvement, and deafness" |
Keratitis–ichthyosis–deafness syndrome (KID syndrome), also known as ichthyosiform erythroderma, corneal involvement, and deafness, presents at birth/infancy and is characterized by progressive corneal opacification, either mild generalized hyperkeratosis or discrete erythematous plaques, and neurosensory deafness.
It is caused by a mutation in connexin 26.
See also
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