203 top medical experts on Dowling-Degos Disease across 24 countries and 8 U.S. states, including 29 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Dowling-Degos Disease: A rare, genetic, hyperpigmentation of the skin disease characterized by adulthood-onset of reticular, reddish-brown to dark-brown, macular and/or comedone-like, hyperkeratotic papules with hypopigmented macules, predominantly affecting flexural areas and, on occasion, progressing to involve trunk and acral regions. Histologically, epidermal acanthosis, thin, branch-like, rete ridges, and a tendency for acantholysis and pigmentary incontinence is observed.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: DDD1,  Dowling-Degos disease 1,  Dowling-Degos-Kitamura Disease,  Kitamura Reticulate Acropigmentation,  Reticular Pigment Anomaly of Flexures,  Reticulate Acropigmentation of Kitamura,  dark dot disease


  

        

                    


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