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  3. Research By Disease

Disease: Otodental dysplasia

  • "Otodental" dysplasia
  • A family with oto-dental dysplasia, odontomas, and pan-tonal hearing disorder
  • A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement
  • Clinical aspects of dental anomalies
  • Clinical, pathological, and genetic evaluations of Chinese patient with otodental syndrome and multiple complex odontoma: Case report
  • Globe-shaped central incisors in a patient with otodental syndrome
  • Globodontia in the Otodental Syndrome: A Rare Defect of Tooth Morphology Occurring with Hearing Loss in an Eight-Year-Old
  • LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations
  • Oto-dental dysplasia
  • Otodental dysplasia
  • Otodental dysplasia: a "new" ectodermal dysplasia
  • Otodental dysplasia: a five year study
  • Otodental syndrome
  • Otodental syndrome
  • Otodental Syndrome
  • Otodental syndrome: a case presentation in a 6-year old child
  • Otodental syndrome: Case report and differential diagnosis with Treacher Collins syndrome
  • Otodental syndrome: three familial case reports
  • Otodental syndrome. A case report
  • Three years of follow-up of otodental syndrome in 3-year-old Chinese boy: a rare case report
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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