Teunissen–Cremers syndrome

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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[edit]

  1. ^ 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. PMID 18440889. doi:10.1016/j.ejmg.2008.02.008.