Otodental sendrom
Otodental displazi
Kalıtsal - AD
Gözlerede koloboma
İşitme sorunları
Yüz uzun
Filtrum uzun
Globodonti (küremsi diş; süt-sürekli kanin ve molarlar)
Pulpa anomalileri
Pulpalarda kalsifikasyon
Süt azılarının ankilozu
Taurodontism
Mine defektleri
Hipodonti
Chen RJ, Chen HS, Lin LM, et al. "Otodental" dysplasia. Oral Surgery, Oral Medicine, Oral Pathology, 66(3):353-358, 1988
Van Doorne L, Wackens G, De Maeseneer M, Deron P. Otodental syndrome: a case report. International Journal of Oral & Maxillofacial Surgery,27: 121-124, 1998
Sedano HO, Moreira LC, de Souza RA, Moleri AB. Otodental syndrome: a case report and genetic considerations. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology & Endodontology, 92(3):312-317, 2001
Vieira H, Gregory-Evans K, Lim N, et al. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1. Investigative Ophthalmology & Visual Science, 43: 2540-2545, 2002
Colter JD, Sedano HO. Otodental syndrome: a case report. Pediatric Dentistry, 27(6):482-485, 2005
Gregory-Evans CY, Moosajee M, Hodges MD, et al. SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma. Human Molecular Genetics, 16: 2482-2493, 2007
Enright S, Humphrys AK, Rea G, James JA. Globodontia in the otodental syndrome: A rare defect of tooth morphology occurring with hearing loss in an eight-year-old. Dental Update, 42(10):927-930 (932), 2015