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Updated: May 13, 2026

Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss
Published on: January 25, 2016
An unusual mucocutaneous syndrome with sensorineural deafness due to connexin 26 mutations
María M Ibáñez1, María M Alcalde, María R Jiménez
1Unidad de Gestión Clínica de Pediatría.
Abstract:
Mutations of the GJB2 gene, which encodes connexin 26, are related to a range of conditions associated with sensorineural deafness and keratinization disorders. We present the case of a newborn girl with sensorineural deafness, erythematous hyperkeratotic plaques on intertriginous areas, and parakeratosis on the oral and esophageal mucosa. She had an F142L mutation in exon 1 of the GJB2 gene, which was described previously in a patient with a similar phenotype.
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