231 top medical experts on Emery-Dreifuss Muscular Dystrophy across 30 countries and 16 U.S. states, including 80 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Emery-Dreifuss Muscular Dystrophy: A heterogenous group of inherited muscular dystrophy without the involvement of nervous system. The disease is characterized by muscular atrophy; muscle weakness; contracture of the elbows; achilles tendon; and posterior cervical muscles; with or without cardiac features. There are several inheritance patterns including X-linked (X chromosome), autosomal dominant (for lmna-associated type see autosomal emery-dreifuss muscular dystrophy), and autosomal recessive gene mutations.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): X-Linked Genetic Diseases (2,304), Muscular Dystrophies (1,543) and Narrower Categories: X-Linked Emery-Dreifuss Muscular Dystrophy (31).
  4. Clinical Trials ClinicalTrials.gov : at least 2 including 1 Recruiting
  5. Synonyms: Emery-Dreifuss Syndrome


  

        

                    


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