Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT

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Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT Andrew J. Griffith, Aqeel A. Chowdhry, Kiyoto Kurima, Linda J. Hood, Bronya Keats, Charles I. Berlin, Robert J. Morell, Thomas B. Friedman The American Journal of Human Genetics Volume 67, Issue 3, Pages 745-749 (September 2000) DOI: 10.1086/303045 Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Figure 1 Pedigree and GJB2 genotypes for the study family segregating nonsyndromic recessive deafness. Blackened symbols denote severe-to-profound sensorineural hearing loss. Audiometric data were not available for individual II:2, although his hearing was subjectively normal. The American Journal of Human Genetics 2000 67, 745-749DOI: (10.1086/303045) Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Figure 2 Pure-tone audiometric thresholds for individuals I:1, who was 52 years of age (A); I:2, who was 47 years of age (B); II:1 (C); II:3 (D); II:4 (E); and II:5 (F). Type B tympanograms (not shown) and normal midline bone conduction thresholds in individual II:5 indicate that the hearing loss is conductive, which is consistent with a known history of bilateral chronic otitis media with effusion. The American Journal of Human Genetics 2000 67, 745-749DOI: (10.1086/303045) Copyright © 2000 The American Society of Human Genetics Terms and Conditions