Teunissen–Cremers syndrome is a genetic disorder that presents with skeleton defects some of which can include the bones of the inner ear, fingers and toes.[1] This can result in conductive hearing loss and finger deformities.[1][2]
References
^ abHirshoren, N; Gross, M; Banin, E; Sosna, J; Bargal, R; Raas-Rothschild, A (Jul–Aug 2008). "P35S mutation in the NOG gene associated with Teunissen–Cremers syndrome and features of multiple NOG joint-fusion syndromes". European Journal of Medical Genetics. 51 (4): 351–7. doi:10.1016/j.ejmg.2008.02.008. PMID18440889.
^Toriello, Helga V.; Smith, Shelley D. (2013). Hereditary Hearing Loss and Its Syndromes. Oxford University Press. p. 405. ISBN9780199313884.
Bert Teunissen, Cor Cremers.
An autosomal dominant inherited syndrome with congenital stapes ankylosis.
Laryngoscope 100: April 1990, 380-384