Conditions Treated
Rheumatological conditions, diseases and disorders we treat include:
Arthritis
- Juvenile idiopathic arthritis (JIA)
- Enthesitis-related JIA
- Oligoarticular JIA
- Polyarticular JIA
- Psoriatic arthritis
- Systemic JIA
- Post-infectious/reactive arthritis
- Other chronic disease-related arthritis/enthesitis
- Celiac disease
- Cystic fibrosis
- Diabetes mellitus
- Inflammatory bowel disease
- Thyroid disease
Autoinflammatory conditions
- Chronic nonbacterial osteomyelitis (CNO), formerly chronic recurrent multifocal osteomyelitis (CRMO)
- Cryopyrin-associated periodic syndromes (CAPS)
- Familial cold autoinflammatory syndrome (FCAS)
- Muckle-Wells syndrome (MWS)
- Neonatal-onset multisystem inflammatory disease (NOMID)
- Periodic fever syndromes
- Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome (CANDLE syndrome)
- Deficiency of interleukin-1 receptor antagonist (DIRA)
- Familial Mediterranean fever (FMF)
- Hyperimmunoglobulin D syndrome (hyper IgD syndrome, HIDS)
- Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA)
- Tumor necrosis factor receptor-associated periodic syndrome (TRAPS)
- Other periodic fever/autoinflammatory syndromes
- Juvenile sarcoidosis/Blau syndrome
- Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome
- Systemic juvenile idiopathic arthritis (sJIA)
- Other unspecified autoinflammatory disorders
Chronic pain syndromes
- Amplified musculoskeletal pain syndrome (AMPS)
- Fibromyalgia
Connective tissue diseases
- Antiphospholipid antibody syndrome (antiphospholipid syndrome, APS)
- Mixed connective tissue disease (MCTD)
- Neonatal lupus
- Scleroderma
- Sjögren's syndrome
- Systemic lupus erythematosus (SLE)
- Relapsing polychondritis
- Undifferentiated connective tissue disease (UCTD)
Inflammatory myopathies
- Idiopathic inflammatory myopathy
- Juvenile dermatomyositis (JDM)
- Juvenile polymyositis (JPM)
Vasculitis
- Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV)
- Eosinophilic granulomatosis with polyangiitis (EGPA)
- Granulomatosis with polyangiitis (GPA)
- Microscopic polyangiitis (MPA)
- Behçet's disease
- Henoch-Schönlein purpura (HSP)
- Idiopathic pulmonary capillaritis
- Kawasaki disease
- Leukocytoclastic vasculitis
- Polyarteritis nodosa
- Takayasu's arteritis
- Other vasculitis
Other conditions and disorders
- Acute rheumatic fever
- Autoimmune sensorineural hearing loss (SNHL)
- Complex aphthosis
- Immunoglobulin G4-related disease (IgG4-RD)
- Joint hypermobility spectrum disorder
- Raynaud’s phenomenon
- Recurrent aphthous stomatitis (RAS. canker sores)
- Recurrent idiopathic pericarditis
- Uveitis