Fig. 1From: Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case reportIllustration and audiometry of KID Argentinean case. a Audioprofile of the patient after cochlear implantation showing good outcome. b The scalp hair was thin, sparse and light-blond. He had aged facial appearance and hypotrichosisBack to article page