KID Syndrome (Keratitis–Ichthyosis–Deafness Syndrome)- AD (few AR), GJB2 gene defect (encoding connexin 26)
- Presents at or near birth with symmetric erythematous hyperkeratotic plaques on knees, elbows, and face; PPK with grainy or stippled appearance
- Congenital sensorineural deafness, vascularizing keratitis with secondary blindness, photophobia, abnormalities of teeth/nails, ↑ infections, ↑ risk (rare) of SCC
| | | | | | KID Syndrome – Konnexin 26 | | | | | |
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