Cochlear implantation in Bjornstad syndrome: a case series with literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Otorhinolaryngology
Link
https://link.springer.com/content/pdf/10.1007/s00405-023-08265-6.pdf
Reference7 articles.
1. Richards KA, Mancini AJ (2002) Three members of a family with pili torti and sensorineural hearing loss: the Bjornstad syndrome. J Am Acad Dermatol 46:301–303. https://doi.org/10.1067/mjd.2002.107969
2. Petit A, Dontenwille MM, Bardon CB, Civatte J (1993) Pili torti with congenital deafness (Bjornstad’s syndrome)–report of three cases in one family, suggesting autosomal dominant transmission. Clin Exp Dermatol 18:94–95. https://doi.org/10.1111/j.1365-2230.1993.tb00983.x
3. Hinson JT, Fantin VR, Schönberger J et al (2007) Missense mutations in the BCS1L gene as a cause of the Björnstad syndrome. N Engl J Med 356:809–819. https://doi.org/10.1056/NEJMoa055262
4. Sennaroglu L, Saatci I (2002) A new classification for cochleovestibular malformations. Laryngoscope 112:2230–2241. https://doi.org/10.1097/00005537-200212000-00019
5. Sennaroglu L (2010) Cochlear implantation in inner ear malformations—a review article. Cochlear Implants Int 11:4–41. https://doi.org/10.1002/cii.416
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