234 top medical experts on Walker-Warburg Syndrome across 31 countries and 11 U.S. states, including 53 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Walker-Warburg Syndrome: Rare autosomal recessive lissencephaly type 2 associated with congenital muscular dystrophy and eye anomalies (e.g., retinal detachment; cataract; microphthalmos). It is often associated with additional brain malformations such as hydrocephaly and cerebellar hypoplasia and is the most severe form of the group of related syndromes (alpha-dystroglycanopathies) with common congenital abnormalities in the brain, eye and muscle development.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Cobblestone Lissencephaly (126), Hereditary Eye Diseases (901), Muscular Dystrophies (1,543).
  4. Clinical Trials ClinicalTrials.gov : at least 2 including 1 Recruiting
  5. Synonyms: Fukuyama Type Cerebromuscular Dystrophy,  Chemke Syndrome,  Fukuyama Congenital Muscular Dystrophy,  Fukuyama Type Congenital Muscular Dystrophy,  Muscle-Eye-Brain Disease,  Fukuyama Type Congenital Muscular Dystrophy,  Warburg Syndrome,  alpha-Dystroglycanopathies


  

        

                    


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