208 top medical experts on Familial cylindromatosis across 28 countries and 11 U.S. states, including 44 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Familial cylindromatosis: A rare genetic disease characterized as an inherited skin tumour predisposition syndrome presenting with skin appendage tumours, namely cylindromas, spiradenomas and trichoepitheliomas
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Ancell-Spiegler cylindromas,  Brooke-Fordyce Trichoepitheliomas,  Brooke-Spiegler syndrome,  Dermal Eccrine Cylindromas,  familial Cylindromatosis,  Dermal Eccrine Cylindroma,  Epithelioma adenoides cysticum of Brooke,  hereditary multiple benign cystic Epithelioma,  Familial Trichoepithelioma,  Hereditary Multiple Benign Cystic Epithelioma,  Multiple Familial Trichoepithelioma,  Spiegler-Brooke syndrome,  Trichoepithelioma multiple familial,  1 Multiple Familial Trichoepithelioma,  Turban tumor syndrome,  Turban tumors


  

        

                    


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