37 top medical experts on Laurin-Sandrow syndrome across 8 countries and 1 U.S. states. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Laurin-Sandrow syndrome: Laurin-Sandrow syndrome (LSS) is characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported, and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: With Absence Of Tibia And Radius Duplication Of Fibula And Ulna,  Fibula ulna duplication tibia radius absence,  Laurin Sandrow syndrome,  Segmental Laurin-Sandrow Syndrome,  Mirror hands and feet with nasal defects,  Mirror-Image Polydactyly,  Sandrow syndrome,  Tetramelic mirror-image polydactyly


  

        

                    


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