SEA syndrome revisited: a longterm followup of children with a syndrome of seronegative enthesopathy and arthropathy

J Rheumatol. 1992 Aug;19(8):1282-5.

Abstract

Thirty-six of the 39 children originally described with the syndrome of seronegative enthesopathy and arthropathy, followed for a mean of 11 years after symptom onset, were found to have had a widely varied clinical course. Twelve of the 23 patients (52%) who originally did not have a seronegative spondyloarthropathy developed definite (6) or possible (6) seronegative spondyloarthropathies. The development of a seronegative spondyloarthropathy was associated with HLA-B27 (p = 0.0004) and the presence of arthritis (rather than arthralgia only) at the time of the original report (p = 0.05). For patients with arthritis, the development of a seronegative spondyloarthropathy was associated with arthritis onset after 5 years of age (p = 0.01).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Causality
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • HLA-B27 Antigen / analysis
  • Humans
  • Infant
  • Joint Diseases / blood
  • Joint Diseases / epidemiology*
  • Joint Diseases / immunology
  • Male
  • Musculoskeletal Diseases / blood
  • Musculoskeletal Diseases / epidemiology*
  • Musculoskeletal Diseases / immunology
  • Risk Factors
  • Spondylitis, Ankylosing / diagnosis
  • Spondylitis, Ankylosing / epidemiology
  • Spondylitis, Ankylosing / immunology
  • Syndrome

Substances

  • HLA-B27 Antigen