There is a high prevalence of children with disabilities, including hearing loss, and the causes of or primary conditions underlying hearing loss vary among children with disabilities. We enrolled 326 children treated at the National Rehabilitation Center for Children with Disabilities during the 30-year period from 1980 to 2011, classified the diseases and causes and compared them by age group to investigate the changes in the types and complications of disabilities in disabled children with hearing loss. In addition, we investigated the presence or absence of hearing loss in children with chromosomal abnormalities. Then, we examined the current state of and issues pertaining to hearing disorder in children and adults with disabilities. The diseases complicated by hearing loss varied, including cerebral palsy, congenital anomalies, mental retardation, chromosomal abnormalities, meningitis, and encephalitis. In addition, low birth weight, congenital cytomegalovirus infection, and auditory neuropathy have been encountered in recent years. Hearing loss was detected in 33 of 64 children with chromosomal abnormalities (51.6%) and in 27 of 56 children with trisomy 21 (48.2%). The frequency of concomitant hearing loss was extremely high in children with chromosomal abnormalities. For children with disabilities, hearing is an extremely important communication method, and early detection and treatment of hearing loss are necessary. The diagnosis, examination, and treatment of hearing loss have advanced. Consequently, the characteristics of disabled children with hearing loss are also becoming more diverse. Therefore, it is necessary to customize aids for hearing and treatment that is tailored to each affected child.
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