Copyright
©The Author(s) 2024.
World J Otorhinolaryngol. Jan 19, 2024; 11(1): 1-17
Published online Jan 19, 2024. doi: 10.5319/wjo.v11.i1.1
Published online Jan 19, 2024. doi: 10.5319/wjo.v11.i1.1
Type | Hearing loss | Vision loss | Vestibular function |
Type 1 | Profound bilateral hearing loss at birth[26,149] | Earlier onset, in the first decade of life[13,26] | Vestibular areflexia at birth[26] |
Type 2 | Moderate to severe hearing loss at birth[13,24] | Late childhood or teens[26] | Normal[44] |
Type 3 | Normal at birth, with progressive loss[28,164] | Commonly in early youth[13,26] | Variable[38] |
- Citation: Cuzzuol BR, Apolonio JS, da Silva Júnior RT, de Carvalho LS, Santos LKS, Malheiro LH, Silva Luz M, Calmon MS, Crivellaro HL, Lemos FFB, Freire de Melo F. Usher syndrome: Genetic diagnosis and current therapeutic approaches. World J Otorhinolaryngol 2024; 11(1): 1-17
- URL: https://www.wjgnet.com/2218-6247/full/v11/i1/1.htm
- DOI: https://dx.doi.org/10.5319/wjo.v11.i1.1