Search
autosomal dominant nonsyndromic sensorineural deafness 28
Genetics:
1) autosomal dominant
2) associated with mutations in GRHL2 gene
Clinical manifestations:
1) mild to moderate hearing loss across most frequencies
2) progresses to severe loss in the higher frequencies by the 5th decade of life
3) age at onset variable, with earliest case documented at 7 years of age
General
familial deafness
Database Correlations
OMIM 608641
References
OMIM :accession 608641