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  3. Research By Disease

Disease: Agnathia-microstomia-synotia

  • Agnathia-microstomia-synotia
  • Agnathia-microstomia-synotia syndrome (otocephaly)
  • Agnathia-synotia-microstomia (otocephaly): a case report in an African woman
  • Agnathia, microstomia, synotia
  • Assessment of Cortical Auditory Function Using Electrophysiological and Neuropsychological Measurements in Children with Bone-Anchored Hearing Aids
  • Cyclopia: isolated and with agnathia-otocephaly complex
  • Otocephaly: Agnathia- Microstomia-Synotia Syndrome- A Rare Congenital Anomaly
  • Plurimalformative syndrome associating trisomy 18 and omphalocele. Case report and review of the literature
  • Prenatal diagnosis of agnathia-otocephaly using sonography and magnetic resonance imaging
  • PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents
  • Severe Agnathia-Otocephaly Complex: Surgical Management and Longitudinal Follow-up From Birth Through Adulthood
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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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