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  3. Research By Disease

Disease: Bazopoulou Kyrkanidou syndrome

  • Epidermal nevus syndrome with development of a mandibular ameloblastoma
  • Glossodynia: personality characteristics and psychopathology
  • Growth retardation, distinct oriental-like facies, glaucoma, brachydactyly, ventricular septal defect and speech disorder. An unknown entity
  • Hyalinosis cutis et mucosae: gingival involvement
  • Hyperbrachycephaly, short face, midface hypoplasia, fusion of cervical vertebrae, radiolucent bone defects, and severe destruction of periodontium--a new syndrome: craniofaciocervical osteoglyphic dysplasia
  • Laband syndrome: a case report
  • Microdontia, hypodontia, short bulbous roots and root canals with strabismus, short stature, and borderline mentality
  • Periodontitis associated with Hajdu-Cheney syndrome
  • Prader-Willi syndrome: report of a case with special emphasis on oral problems
  • Pure de novo partial trisomy 6p in a girl with craniosynostosis
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About CheckOrphan

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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