64 top medical experts on Palmoplantar Keratoderma with Deafness across 8 countries and 1 U.S. states, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Palmoplantar Keratoderma with Deafness: Palmoplantar keratoderma-deafness syndrome is a keratinization disorder characterized by focal or diffuse palmoplantar keratoderma. A patchy distribution is observed with accentuation on the thenars, hypothenars and the arches of the feet. The disease becomes apparent in infancy and is associated with sensorineural hearing loss that shows a variable age of onset. Due to genetic and clinical similarities, it has been proposed that palmoplantar keratoderma-deafness syndrome, knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome and keratoderma hereditarium mutilans may represent variants of one broad disorder of syndromic deafness with heterogeneous phenotype. The disease is transmitted in an autosomal dominant manner with incomplete penetrance.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Diffuse palmoplantar keratoderma with deafness,  Focal palmoplantar keratoderma with sensorineural deafness,  Hereditary palmoplantar keratoderma with deafness,  Keratoderma palmoplantar deafness,  with deafness Keratoderma palmoplantar,  With Deafness Palmoplantar Keratoderma,  Palmoplantar Hyperkeratosis-Deafness Syndrome,  Palmoplantar Hyperkeratosis-Hearing Loss Syndrome,  Palmoplantar Keratoderma-Deafness Syndrome,  Palmoplantar Keratoderma-Hearing Loss Syndrome,  Palmoplantar keratoderma and sensorineural deafness,  Ppk with Deafness,  Ppk-Deafness Syndrome


  

        

                    


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