Overview
Oligoarticular juvenile idiopathic arthritis (JIA) with anti-nuclear antibodies (ANA) was a proposed subclassification of juvenile idiopathic arthritis that has since been marked as OBSOLETE in the Orphanet classification system (Orphanet code 247839). Oligoarticular JIA is the most common subtype of juvenile idiopathic arthritis, characterized by chronic joint inflammation affecting four or fewer joints during the first six months of disease. The presence of ANA positivity in these patients was historically noted as a distinguishing feature associated with an increased risk of chronic anterior uveitis (inflammation of the eye), younger age of onset, and a female predominance. The musculoskeletal system is primarily affected, with joints such as the knees, ankles, and wrists most commonly involved, leading to pain, swelling, and stiffness. The eyes are also at significant risk due to ANA-associated uveitis, which can lead to vision loss if not detected and treated early. This specific designation has been rendered obsolete as classification systems for JIA have evolved. Current approaches, including the International League of Associations for Rheumatology (ILAR) classification and proposed revisions by the Pediatric Rheumatology International Trials Organisation (PRINTO), have moved toward different categorization frameworks. ANA positivity is now recognized as a cross-cutting feature across multiple JIA categories rather than a defining criterion for a separate subtype. Treatment for oligoarticular JIA generally includes nonsteroidal anti-inflammatory drugs (NSAIDs), intra-articular corticosteroid injections, and disease-modifying antirheumatic drugs (DMARDs) such as methotrexate. Biologic agents, particularly TNF inhibitors, may be used in refractory cases. Regular ophthalmologic screening remains essential for ANA-positive patients to detect and manage uveitis early.
Also known as:
Multifactorial
Caused by a mix of several genes and environmental factors
Childhood
Begins in childhood, roughly ages 1 to 12
FDA & Trial Timeline
1 eventRinvoq: FDA approved
treatment of patients 2 years of age and older with active polyarticular juvenile idiopathic arthritis who have had an inadequate response or intolerance to one or more tumor necrosis factor (TNF) blockers, and for the treatment of pediatric patients 2 years of age and older with active psoriatic arthritis who have had an inadequate response or intolerance to one or more TNF blockers
Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
Treatments
No FDA-approved treatments are currently listed for OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies.
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Specialists
View all specialists →No specialists are currently listed for OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies.
Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies.
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Common questions about OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies
What is OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies?
Oligoarticular juvenile idiopathic arthritis (JIA) with anti-nuclear antibodies (ANA) was a proposed subclassification of juvenile idiopathic arthritis that has since been marked as OBSOLETE in the Orphanet classification system (Orphanet code 247839). Oligoarticular JIA is the most common subtype of juvenile idiopathic arthritis, characterized by chronic joint inflammation affecting four or fewer joints during the first six months of disease. The presence of ANA positivity in these patients was historically noted as a distinguishing feature associated with an increased risk of chronic anterio
How is OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies inherited?
OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies follows a multifactorial inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.
At what age does OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies typically begin?
Typical onset of OBSOLETE: Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies is childhood. Age of onset can vary across affected individuals.