211 top medical experts on Burnett Schwartz Berberian syndrome across 28 countries and 17 U.S. states, including 63 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Burnett Schwartz Berberian syndrome: A rare genetic skin disease characterized by childhood onset of follicular keratotic papules slowly progressing to characteristic ''honeycomb'' atrophy on the cheeks, preauricular area, and forehead. Less frequently, the condition may affect also the upper lip, ears, or limbs. Additional features include facial erythema, milia, and follicular plugs.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: X-linked 2 hypoplastic-hypomaturation Amelogenesis imperfecta,  Atrophodermia Reticulata Symmetrica Faciei,  Atrophodermia reticulata,  Atrophodermia vermiculata,  Folliculitis ulerythematosa,  Folliculitis ulerythematosa reticulata,  Honeycomb atrophy,  Keratosis Pilaris Atrophicans Facies,  Keratosis pilaris,  Ulerythema ophryogenes,  Ulerythema ophryogenes with multiple congenital anomalies,  Ulerythema ophryogenesis


  

        

                    


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