Fig. 1
From: Connexin-26–associated deafness: Phenotypic variability and progression of hearing loss
Patient demographics. A, Flowchart of patient inclusion. Fifty-two patients had autosomal recessive disease-causing mutations in GJB2; of these, 33 had serial audiometric data. B, Demographics. Comorbidities identified: keratitis-ichthyosis-deafness syndrome, cleft lip/palate, and renal disease. Computed tomography (CT) abnormalities: enlarged vestibular aqueduct and asymmetry of the internal auditory canal.
