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Familial Otosclerosis Associated with Osteogenesis Imperfecta: A Case Report
Otosclerosis, a hereditary disorder characterized by disordered resorption and deposition of bone, results in progressive hearing loss. Osteogenesis imperfecta (OI) is a genetic disorder characterized by recurrent fractures, blue sclera, and varying degrees of hearing impairment; and is a known risk...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Audiological Society and Korean Otological Society
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524114/ https://www.ncbi.nlm.nih.gov/pubmed/34167184 http://dx.doi.org/10.7874/jao.2021.00122 |