202 top medical experts on Auriculo-condylar syndrome across 26 countries and 10 U.S. states, including 18 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Auriculo-condylar syndrome: A rare, genetic dysostosis with predominant craniofacial involvement characterized by bilateral external ear malformations, mandibular condyle hypoplasia, microstomia, micrognathia, microglossia and facial asymmetry. Additional manifestations include hypotonia, ptosis, cleft palate, full cheeks, developmental delay, hearing impairment and respiratory distress. Significant intra- and interfamilial phenotypic variation has been reported.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: ARCND1,  Auriculocondylar syndrome,  Auriculocondylar syndrome 1,  Ears prominent and constricted,  Question Mark Ears Syndrome,  Question mark ear,  Question-Mark Ear Syndrome


  

        

                    


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