autosomal dominant nonsyndromic sensorineural deafness 22

Pathology

• sensorineural deafness

Genetics

• autosomal dominant
• associated with mutations in gene for myosin 6

Clinical manifestations

• progressive & postlingual, with onset during childhood
• by the age of approximately 50 years, affected individuals invariably have profound sensorineural deafness

More general terms

• familial deafness

Database

• OMIM: https://mirror.omim.org/entry/606346