122 top medical experts on Keratosis palmoplantaris papulosa across 15 countries and 1 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Keratosis palmoplantaris papulosa: Punctate palmoplantar keratoderma type I is a rare condition that affects the skin. It is a sub-type of punctate palmoplantar keratoderma .Signs and symptoms typically begin in early adolescence or later and include hard, round bumps of thickened skin on the palms of the hands and soles of the feet. These bumps can cause pain in some people.The condition is usually inherited in an autosomal dominant manner and can be caused by a mutation in the AAGAB gene .Treatment options may include removal of the thickened skin by a doctor or using a cream on the affected area. Some people have used surgical approaches consisting of excision and skin grafting.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Buschke Fischer Brauer syndrome,  Punctate Type I Palmoplantar Keratoderma,  palmoplantar punctate type 1 Keratoderma,  Buschke-Fischer-Brauer type Keratodermia palmoplantaris papulosa,  Type I punctate palmoplantar keratoderma


  

        

                    


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