OÖ

 

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

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