familial deafness

Pathology: 1) arrhythmias, sudden death 2) sensorineural hearing loss

Specific

Alexander's deafness autosomal dominant deafness type 11 autosomal dominant deafness type 13 autosomal dominant neurosensory deafness autosomal dominant neurosensory deafness 36 (DFNA36) autosomal dominant nonsyndromic sensorineural deafness 14 (deafness autosomal dominant type 6) autosomal dominant nonsyndromic sensorineural deafness 15 autosomal dominant nonsyndromic sensorineural deafness 22 autosomal dominant nonsyndromic sensorineural deafness 23 autosomal dominant nonsyndromic sensorineural deafness 28 autosomal dominant nonsyndromic sensorineural deafness 48 autosomal dominant nonsyndromic sensorineural deafness 9 autosomal dominant sensorineural deafness type 10 autosomal dominant sensorineural deafness type 9 autosomal recessive neurosensory deafness deafness autosomal dominant type 1 (DFNA1) deafness autosomal dominant type 20 deafness autosomal dominant type 2A (DFNA2A) deafness autosomal dominant type 4B hereditary nonsyndromic hearing loss mitochondrial sensorineural deafness nonsyndromic recessive deafness X-linked deafness

General

deafness developmental disorder genetic disease of the auditory system

References

Harrison's Principles of Internal Medicine, 13th ed. Isselbacher et al (eds), McGraw-Hill Inc. NY, 1994, pg 1038