200 top medical experts on Shprintzen Golberg craniosynostosis across 20 countries and 8 U.S. states, including 24 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Shprintzen Golberg craniosynostosis: Shprintzen-Goldberg syndrome (SGS) is a very rare genetic disorder characterized by craniosynostosis, craniofacial and skeletal abnormalities, marfanoid habitus, cardiac anomalies, neurological abnormalities, and intellectual disability.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: type 1 Craniosynostosis and Marfanoid disorder,  Craniosynostosis with arachnodactyly and abdominal hernias,  Type I Marfanoid Disorder With Craniosynostosis,  Marfanoid craniosynostosis syndrome,  Marfanoid-Craniosynostosis Syndrome,  Shprintzen Golberg craniosynostosis syndrome,  Shprintzen-Goldberg Craniosynostosis Syndrome,  Shprintzen-Goldberg Syndrome


  

        

                    


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