87 top medical experts on Jacobs syndrome across 11 countries and 8 U.S. states, including 9 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Jacobs syndrome: A rare, genetic, rheumatologic disease characterized by congenital or early-onset camptodactyly and symmetrical, polyarticular, non-inflammatory, large joint arthropathy with synovial hyperplasia, as well as progressive coxa vara deformity and, occasionally, non-inflammatory pericarditis.
  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: Arthropathy camptodactyly syndrome,  Arthropathy-Camptodactyly Syndrome,  Camptodactyly arthropathy pericarditis syndrome,  Camptodactyly-Arthropathy-Pericarditis Syndrome,  Camptodactyly-arthropathy-coxa vara-pericarditis syndrome,  Congenital familial hypertrophic synovitis,  familial Fibrosing serositis,  Congenital Familial Hypertrophic Synovitis,  Pericarditis arthropathy camptodactyly syndrome,  Pericarditis-Arthropathy-Camptodactyly Syndrome


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