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. Author manuscript; available in PMC: 2022 Nov 1.
Published in final edited form as: Int J Pediatr Otorhinolaryngol. 2021 Aug 16;150:110872. doi: 10.1016/j.ijporl.2021.110872

Table 1.

Syndromic Forms od Deafness identified Through NexGen Sequencing.

Condition Number of cases diagnosed Diagnostic yield
Usher Syndrome 98 9.98%
Pendred Syndrome or autosomal recessive non-syndromic hearing loss 46 4.68%
Deafness Infertility Syndrome or female autosomal recessive non-syndromic hearing loss 37 3.77%
Branchiootorenal syndrome 16 1.63%
Waardenburg Syndrome 9 0.92%
Stickler Syndrome 4 0.41%