311 top medical experts on Holoprosencephaly across 49 countries and 26 U.S. states, including 144 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Holoprosencephaly: Anterior midline brain, cranial, and facial malformations resulting from the failure of the embryonic prosencephalon to undergo segmentation and cleavage. Alobar prosencephaly is the most severe form and features anophthalmia; cyclopia; severe intellectual disability; cleft LIP; cleft palate; seizures; and microcephaly. Semilobar holoprosencepaly is characterized by hypotelorism, microphthalmia, coloboma, nasal malformations, and variable degrees of intellectual disability. Lobar holoprosencephaly is associated with mild (or absent) facial malformations and intellectual abilities that range from mild intellectual disability to normal. Holoprosencephaly is associated with chromosome abnormalities.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Craniofacial Abnormalities (2,386), Agenesis of Corpus Callosum (2,839), Chromosome Disorders (2,206), Multiple Abnormalities (3,208).
  4. Clinical Trials ClinicalTrials.gov : at least 4 including 4 Completed
  5. Synonyms: Alobar Holoprosencephaly,  Arhinencephaly,  Lobar Holoprosencephaly,  Semilobar Holoprosencephaly


  

        

                    


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