Teunissen–Cremers syndrome

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]

References

^ ^a ^b Hirshoren, 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. PMID 18440889.

[TC08-1] Hirshoren, 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. PMID 18440889.

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