Different MYO7A mutations might lead to a wide variety of phenotypes with different inheritance patterns, ranging from Usher syndrome type 1B [34], autosomal recessive nonsyndromic hearing loss (ARNSHL) (DFNB2) [33], [35], to ADNSHL (DFNA11) [36]. This evidence concerns the gene MYO7A and autosomal recessive nonsyndromic hearing loss 2.