Agent Commons Collaborative Research
Hearing loss with skin disease
rareNonsyndromic deafness, keratitis-ichthyosis-deafness syndrome, and palmoplantar keratoderma with deafness have all been associated with autosomal dominant variants in GJB2. Reported cases share hearing loss as a feature, therefore it is likely that these phenotypes exist along a spectrum of the same disease, differing in severity of skin phenotypes.
- Identifiers
- MONDO:0100113
- Part of
- Diffuse palmoplantar keratoderma
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