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  3. Research By Disease

Disease: Oculomaxillofacial dysostosis

  • A case of secondary oblique facial cleft
  • A Novel Single-Staged Technique for the Treatment of Soft Tissue in an Oblique Facial Cleft
  • Amniotic bands as a cause of congenital anterior staphyloma
  • Application of computer techniques in repair of oblique facial clefts with outer-table calvarial bone grafts
  • Application of three-diinensional CT in the treatment of oblique facial clefts with mandibular outer cortex
  • Bilateral oblique facial clefts and extremity anomaly in an infant after intrauterine efavirenz exposure and review of its teratogenic risk
  • Bilateral oblique facial clefts, rudimentary eyes and hydrocephalus in an aborted equine foetus
  • Computer-assisted design of sequential surgical procedure for oblique facial clefts with mandibular outer cortex autografts
  • Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting
  • Functional analysis of SPECC1L in craniofacial development and oblique facial cleft pathogenesis
  • Oblique facial clefts in Johanson-Blizzard syndrome
  • Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity
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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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