137 top medical experts on Hypertelorism with esophageal abnormality and hypospadias across 19 countries and 6 U.S. states, including 9 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hypertelorism with esophageal abnormality and hypospadias: A rare X-linked congenital midline malformation syndrome characterized by hypertelorism, laryngo-tracheo-esophageal defects and hypospadias.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: Autosomal Dominant Opitz Syndrome (ADOS),  Opitz Phenotype Chromosome 22q11.2 Deletion Syndrome,  Hypertelorism hypospadias syndrome,  Hypertelorism with Esophageal Abnormalities and Hypospadias,  Hypertelorism-Hypospadias Sydrome,  Hypospadias-Dysphagia Syndrome,  syndrome Hypospadias-dysphagia,  Opitz BBB Syndrome,  Opitz BBB-G Syndrome,  Opitz BBBG syndrome,  Opitz G Syndrome,  Opitz G-BBB Syndrome,  Autosomal Dominant Opitz GBBB Syndrome,  Type II Opitz GBBB Syndrome,  Type II Opitz Oculogenitolaryngeal Syndrome,  Opitz-Frias syndrome,  Type II Opitz-G Syndrome,  type 2 Opitz-G syndrome,  Telecanthus with associated abnormalities


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