335 top medical experts on Loeys-Dietz Syndrome across 35 countries and 24 U.S. states, including 214 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Loeys-Dietz Syndrome: An autosomal dominant aneurysm with multisystem abnormalities caused by increased TGF-beta signaling due to mutations in type I or II of TGF-beta receptor. Additional craniofacial features include cleft palate; craniosynostosis; hypertelorism; or bifid uvula. Phenotypes closely resemble marfan syndrome; Marfanoid craniosynostosis syndrome (Shprintzen-Goldberg syndrome); and ehlers-danlos syndrome.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Genetic Diseases (2,477), Craniofacial Abnormalities (2,386), Aortic Aneurysm (3,983), Dissecting Aneurysm (4,962), Multiple Abnormalities (3,208).
  4. Clinical Trials ClinicalTrials.gov : at least 7 including 2 Completed, 3 Recruiting
  5. Synonyms: Loeys-Dietz Aortic Aneurysm Syndrome


  

        

                    


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