190 top medical experts on Oculodigitoesophagoduodenal syndrome across 11 countries and 7 U.S. states, including 12 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Oculodigitoesophagoduodenal syndrome: A rare genetic, congenital malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies (brachymesophanlangy, fifth finger clinodactyly, syndactyly of toes and hypoplastic thumbs), mild learning deficit and short palpebral fissures. The two subtypes are clinically distinguished by the presence (type 1) or absence (type 2) gastrointestinal atresia.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Brunner Winter syndrome,  Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum,  Feingold syndrome,  MMT Syndrome,  MODED syndrome Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome,  Microcephaly and Digital Abnormalities with Normal Intelligence,  and Tracheoesophageal Fistula Syndrome Mental Retardation Microcephaly,  Microcephaly-Mesobrachyphalangy-Tracheoesophageal Fistula (MMT) Syndrome,  Microcephaly-Oculo-Digito-Esophageal-Duodenal (MODED) Syndrome,  Microcephaly-oculo-digito-esophageal-duodenal syndrome,  ODED Syndrome,  Oculo-Digito-Esophagoduodental (ODED) Syndrome


  

        

                    


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