223 top medical experts on Mowat-Wilson syndrome across 33 countries and 12 U.S. states, including 46 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Mowat-Wilson syndrome: A rare multiple congenital anomaly syndrome characterized by a distinct facial phenotype, intellectual disability, epilepsy, Hirschsprung disease (HSCR) and variable congenital malformations.
  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: Hirschsprung Disease-Mental Retardation Syndrome,  Hirschsprung disease mental retardation syndrome,  with Or without Hirschsprung Disease and Distinct Facial Features Mental Retardation Microcephaly

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