711 top medical experts on X-Linked Genetic Diseases across 45 countries and 41 U.S. states, including 671 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. X-Linked Genetic Diseases: Genetic diseases that are linked to gene mutations on the X chromosome in humans (X chromosome, human) or the X chromosome in other species. Included here are animal models of human X-linked diseases.
  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 (1,340) and Narrower Categories: Aicardi Syndrome (206), Androgen-Insensitivity Syndrome (80), Anhidrotic Ectodermal Dysplasia 1 (341), Barth Syndrome (271), Choroideremia (327), Chronic Granulomatous Disease (663), Dent Disease (193), Duchenne Muscular Dystrophy (1,945), Dyskeratosis Congenita (646), Emery-Dreifuss Muscular Dystrophy (347), Fabry Disease (936), Focal Dermal Hypoplasia (226), Glycogen Storage Disease Type IIb (276), Hemophilia B (638), Isolated Noncompaction of the Ventricular Myocardium (449), Oculocerebrorenal Syndrome (216), Ornithine Carbamoyltransferase Deficiency Disease (426), Pelizaeus-Merzbacher Disease (422), Type 1 Hyper-IgM Immunodeficiency Syndrome (145), Wiskott-Aldrich Syndrome (96), X-Linked Bulbo-Spinal Atrophy (263), X-Linked Combined Immunodeficiency Diseases (384), X-Linked Ichthyosis (163), X-Linked Mental Retardation (1,180).
  4. Clinical Trials ClinicalTrials.gov : at least 29 including 3 Active, 11 Completed, 6 Recruiting


  

        

                    


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