200 top medical experts on Strudwick syndrome across 27 countries and 12 U.S. states, including 15 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Strudwick syndrome: Spondyloepimetaphyseal dysplasia congenita, Strudwick type is characterized by disproportionate short stature from birth (with a very short trunk and shortened limbs) and skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clubfoot, and abnormal epiphyses or metaphyses).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Dappled metaphysis syndrome,  Sed Strudwick,  Strudwick Type Semd,  Strudwick Type Smed,  Type I Smed,  Strudwick type Spondyloepimetaphyseal dysplasia,  Strudwick Type Spondylometaepiphyseal Dysplasia Congenita,  Spondylometaphyseal Dysplasia,  Spondylometaphyseal Dysplasia (Smd)


  

        

                    


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