570 top medical experts on Genetic Skin Diseases across 60 countries and 35 U.S. states, including 415 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Genetic Skin Diseases: Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Skin Diseases (3,308), Inborn Genetic Diseases (2,477) and Narrower Categories: Albinism (840), Atopic Dermatitis (3,715), Benign Familial Pemphigus (670), Congenital Ichthyosiform Erythroderma (975), Cutis Laxa (1,184), Darier Disease (1,345), Dyskeratosis Congenita (1,337), Ectodermal Dysplasia (885), Ehlers-Danlos Syndrome (972), Epidermolysis Bullosa (2,065), Erythrokeratodermia Variabilis (257), Erythropoietic Porphyria (381), Hepatic Porphyrias (226), Hereditary Autoinflammatory Diseases (2,464), Hereditary Mucosal Leukokeratosis (109), Ichthyosis Bullosa of Siemens (32), Ichthyosis Vulgaris (194), Incontinentia Pigmenti (842), Lipoid Proteinosis of Urbach and Wiethe (425), Monilethrix (137), Muir-Torre Syndrome (553), Netherton Syndrome (605), Palmoplantar Keratoderma (2,414), Porokeratosis (1,207), Prolidase Deficiency (192), Pseudoxanthoma Elasticum (1,267), Rothmund-Thomson Syndrome (378), Sjogren-Larsson Syndrome (340), Systemic Hyalinosis (296), Trichothiodystrophy Syndromes (414), X-Linked Ichthyosis (329), Xeroderma Pigmentosum (1,748).
  4. Clinical Trials ClinicalTrials.gov : at least 13 including 2 Active, 6 Completed, 2 Recruiting


  

        

                    


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