36 top medical experts on autosomal recessive Ichthyosis with hypotrichosis across 4 countries and 6 U.S. states, including 4 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. autosomal recessive Ichthyosis with hypotrichosis: Ichthyosis-hypotrichosis syndrome is characterised by congenital ichthyosis and hypotrichosis. It has been described in three members of a consanguineous Arab Israeli family. The syndrome is transmitted as an autosomal recessive trait and is caused by a missense mutation in the ST14 gene, encoding the recently identified protease, matriptase. Analysis of skin samples from the patients suggests that this enzyme plays a role in epidermal desquamation.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Autosomal recessive ichthyosis with hypotrichosis,  and Hypohidrosis Hypotrichosis Follicular Atrophoderma Ichthyosis


  

        

                    


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