Intermediate uveitis

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18Specialists8Treatment centers

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Overview

Intermediate uveitis is a chronic inflammatory eye disease characterized by inflammation primarily affecting the vitreous cavity (the gel-filled space inside the eye) and the peripheral retina. It is also known as pars planitis when it occurs in its idiopathic form with characteristic snowbank or snowball opacities. The condition falls within the broader category of uveitis, which refers to inflammation of the uveal tract of the eye. Intermediate uveitis accounts for approximately 10-20% of all uveitis cases and predominantly affects younger adults and children. Key symptoms include floaters (spots or strands in the visual field), blurred vision, and, less commonly, mild eye pain or redness. Many patients experience a gradual, painless decrease in visual acuity. The disease can be bilateral in a significant proportion of cases. Complications may include cystoid macular edema (swelling of the central retina), cataracts, vitreous opacities, epiretinal membrane formation, and, in severe cases, retinal detachment, all of which can lead to significant vision loss if untreated. Intermediate uveitis can be idiopathic or associated with systemic conditions such as multiple sclerosis, sarcoidosis, or certain infectious diseases including tuberculosis and Lyme disease. A thorough systemic workup is often recommended to identify any underlying cause. The condition is thought to involve immune-mediated mechanisms, though the precise pathogenesis remains incompletely understood. Treatment depends on severity and typically follows a stepwise approach. Mild cases may be observed without treatment. For visually significant disease, corticosteroids (periocular injections or systemic) are the first-line therapy. Steroid-sparing immunosuppressive agents such as methotrexate, mycophenolate mofetil, or azathioprine are used for chronic or refractory cases. Biologic agents, including anti-TNF therapies such as adalimumab, have shown efficacy in refractory intermediate uveitis. Intravitreal sustained-release corticosteroid implants (such as fluocinolone acetonide or dexamethasone implants) are also used. Pars plana vitrectomy may be considered in cases with persistent vitreous opacities or complications. With appropriate management, many patients can achieve good long-term visual outcomes, though the disease often follows a chronic relapsing course requiring prolonged treatment.

Also known as:

Clinical phenotype terms— hover any for plain English:

Psoriasiform dermatitisHP:0003765Chronic infectionHP:0031035Macular scarHP:0200056Macular edemaHP:0040049Band keratopathyHP:0000585Posterior synechiae of the anterior chamberHP:0011484Cystoid macular edemaHP:0011505Anterior uveitisHP:0012122Vitreous hazeHP:0030652Vitreous snowballsHP:0030661Epiretinal membraneHP:0100014Optic neuritisHP:0100653Vitreous floatersHP:0100832
Inheritance

Multifactorial

Caused by a mix of several genes and environmental factors

Age of Onset

Childhood to adulthood

Can begin any time from childhood through adulthood

Orphanet ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Intermediate uveitis.

View clinical trials →

No actively recruiting trials found for Intermediate uveitis at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Intermediate uveitis community →

Specialists

18 foundView all specialists →
NM
Nisha Acharya, MD MS
Specialist
PI on 4 active trials2 Intermediate uveitis publications
AM
Arnd Heiligenhaus, MD
Specialist
PI on 3 active trials1 Intermediate uveitis publication
TM
Thomas Ciulla, MD
CARMEL, IN
Specialist
PI on 8 active trials
RM
Regina Max, MD
Specialist
PI on 1 active trial
QM
Quan D Nguyen, MD, MSc
Specialist
PI on 5 active trials
FF
Friederike Mackensen, MD, FEBO
Specialist
PI on 1 active trial
SS
Samir S Shoughy
Specialist
PI on 2 active trials
TM
Thomas Cuilla, MD, MBA
Specialist
PI on 1 active trial
AP
Andy Payne
Specialist
PI on 1 active trial17 Intermediate uveitis publications
MP
Matthias D Becker, MD, PhD,FEBO
Specialist
PI on 1 active trial
EM
Emily Y Chew, M.D.
BETHESDA, MD
Specialist
PI on 8 active trials
BP
Brendan Johnson, PhD
Specialist
PI on 1 active trial
HM
Hatice N Sen, M.D.
RIVERSIDE, CA
Specialist
PI on 8 active trials
HM
Hatice Nida Sen, MD, MHSc
RIVERSIDE, CA
Specialist
PI on 2 active trials
AM
Antoine AB BREZIN, MD
Specialist
PI on 1 active trial1 Intermediate uveitis publication
GJ
Glenn J Jaffe
DURHAM, NC
Specialist
PI on 4 active trials

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Intermediate uveitis.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Intermediate uveitis

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Caregiver Resources

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Learn how rare disease patients may qualify for SSDI/SSI benefits.

Common questions about Intermediate uveitis

What is Intermediate uveitis?

Intermediate uveitis is a chronic inflammatory eye disease characterized by inflammation primarily affecting the vitreous cavity (the gel-filled space inside the eye) and the peripheral retina. It is also known as pars planitis when it occurs in its idiopathic form with characteristic snowbank or snowball opacities. The condition falls within the broader category of uveitis, which refers to inflammation of the uveal tract of the eye. Intermediate uveitis accounts for approximately 10-20% of all uveitis cases and predominantly affects younger adults and children. Key symptoms include floaters (

How is Intermediate uveitis inherited?

Intermediate uveitis follows a multifactorial inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Intermediate uveitis typically begin?

Typical onset of Intermediate uveitis is childhood to adulthood. Age of onset can vary across affected individuals.

Which specialists treat Intermediate uveitis?

18 specialists and care centers treating Intermediate uveitis are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.