201 top medical experts on Laminopathies across 17 countries and 9 U.S. states, including 22 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Laminopathies: Congenital neuromuscular and muscular dystrophy diseases associated with mutations in the lamin type A (Lamin A/C or lmna gene). It includes cardiomyopathy, dilated, 1A; charcot-marie-tooth disease, type 2B1; emery-dreifuss muscular dystrophy, types 2 and 3; hutchinson-gilford progeria syndrome; lipodystrophy, familial partial, type 2; Malouf syndrome; Mandibuloacral dysplasia; lmna-related muscular dystrophy; Restrictive dermopathy, lethal; Heart-hand syndrome, Slovenian type.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Genetic Diseases (2,477) and Narrower Categories: Dilated Cardiomyopathy (4,540), Familial Partial Lipodystrophy (565), Progeria (2,405).
  4. Clinical Trials ClinicalTrials.gov : at least 5 including 2 Recruiting
  5. Synonyms: LMNA-Associated Diseases,  LMNA-Linked Diseases


  

        

                    


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