49 top medical experts on type 2 Rhizomelic chondrodysplasia punctata across 4 countries and 3 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. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  2. Synonyms: Due To Dihydroxyacetonephosphate Acyltransferase Deficiency Rhizomelic Chondrodysplasia Punctata,  due to DHAPAT deficiency rhizomelic Chondrodysplasia punctata,  DHAPAT deficiency,  Dihydroxyacetonephosphate acyltransferase deficiency,  GNPAT deficiency,  Glyceronephosphate O-Acyltransferase Deficiency,  Glyceronephosphate acyltransferase deficiency,  Human dihydroxyacetonephosphate acyltransferase deficiency,  Peroxisomal dihydroxyacetonephosphate acyltransferase deficiency,  Type 2 rhizomelic chondrodysplasia punctata


  

        

                    


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