123 top medical experts on Stuve-Wiedemann syndrome across 16 countries and 3 U.S. states, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Stuve-Wiedemann syndrome: Stüve-Wiedemann syndrome (SWS) is a rare autosomal recessive congenital primary skeletal dysplasia, characterized by small stature, bowing of the long bones, camptodactyly, hyperthermic episodes, respiratory distress/apneic episodes and feeding difficulties that usually lead to early mortality.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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  • Synonyms: Schwartz Jampel syndrome neonatal,  Schwartz Jampel type 2 syndrome,  Neonatal Schwartz-Jampel Syndrome,  Type 2 Schwartz-Jampel Syndrome,  Stuve-Wiedemann-Schwartz-Jampel type 2 syndrome


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