Question 1

What is adult-onset Still disease?

Accepted Answer

Adult-onset Still disease is a rare inflammatory multisystem disorder. It is characterized by fever of unknown origin, joint pain or arthritis, a typical skin rash, and high levels of white blood cells. This condition affects multiple systems of the body, leading to varied symptoms that can be challenging to diagnose and manage.

Question 2

What are the symptoms of adult-onset Still disease?

Accepted Answer

People with this condition may experience a persistent fever, joint pain or arthritis, a characteristic skin rash, and an increased number of white blood cells. These symptoms can vary in intensity over time.

Question 3

What causes adult-onset Still disease?

Accepted Answer

Information about causes is currently limited for this condition.

Question 4

How rare is adult-onset Still disease?

Accepted Answer

adult-onset Still disease is classified as uncommon. The estimated prevalence is approximately 1-9 in 100,000. Because rare disease data can be limited, actual numbers may differ from published estimates.

Question 5

How is adult-onset Still disease diagnosed?

Accepted Answer

Information about diagnosis is currently limited for this condition.

Question 6

Are there treatments for adult-onset Still disease?

Accepted Answer

Information about treatment is currently limited for this condition.

Question 7

What complications can arise from adult-onset Still disease?

Accepted Answer

Adult-onset Still disease can lead to complications such as joint damage due to ongoing inflammation. Some people may also experience issues with their organs, like the heart or liver, as the disease affects multiple systems. It's important to monitor these potential complications with your doctor.

Question 8

How does adult-onset Still disease affect daily life?

Accepted Answer

Living with adult-onset Still disease can be challenging due to symptoms like joint pain and fever. These symptoms may affect your ability to work, participate in activities, or even perform daily tasks. Finding ways to manage these symptoms with your healthcare team can help improve your quality of life.

Question 9

What is the prognosis for someone with adult-onset Still disease?

Accepted Answer

The prognosis for adult-onset Still disease can vary greatly from person to person. Some people may experience periods of remission, while others might have ongoing symptoms. Regular follow-up with a healthcare provider is essential to manage the disease effectively.

Question 10

Are there specific specialists I should see for adult-onset Still disease?

Accepted Answer

It is often recommended to see a rheumatologist for adult-onset Still disease, as they specialize in inflammatory conditions. You may also need to work with other specialists, like a dermatologist for skin issues or a hematologist for blood-related concerns. Collaborating with a team of healthcare providers can help you manage the disease better.

Brand Name	Generic Name	Sponsor	Designated	Exclusivity End	Designation Status
tadekinig alfa	tadekinig alfa	AB2 Bio Ltd	2017	—	Designated
Interleukin-1 Trap	Interleukin-1 Trap	Regeneron Pharmaceuticals, Inc.	2005	—	Designated

Kisho

adult-onset Still disease

Overview

Diagnosis

Treatment

Approved Therapies

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Questions for Your Care Team

Questions for Your Care Team

FAQ

Frequently Asked Questions

Guideline-Recommended Treatments

Orphan Drug Designations

Clinical Trials

Recent Publications

Latest News & Developments

Still's disease and malignancies: insights into the balance between inflammatory enhancement and immune control. Data from the International AIDA Network Still's Disease Registry.

Adult-onset Still Disease Flare 5 Days Following Poly-l-lactic Acid Injection: A Cautionary Tale for Aesthetic Practice.

Secondary pulmonary alveolar proteinosis mimicking progression of interstitial lung disease during treatment for adult-onset still's disease: An autopsy case report.

adult-onset Still disease

Overview

Diagnosis

Treatment

Approved Therapies

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

FAQ

Frequently Asked Questions

What is adult-onset Still disease?

What are the symptoms of adult-onset Still disease?

What causes adult-onset Still disease?

How rare is adult-onset Still disease?

How is adult-onset Still disease diagnosed?

Are there treatments for adult-onset Still disease?

What complications can arise from adult-onset Still disease?

How does adult-onset Still disease affect daily life?

What is the prognosis for someone with adult-onset Still disease?

Are there specific specialists I should see for adult-onset Still disease?

Guideline-Recommended Treatments

Orphan Drug Designations

Clinical Trials

Recent Publications

Latest News & Developments

Still's disease and malignancies: insights into the balance between inflammatory enhancement and immune control. Data from the International AIDA Network Still's Disease Registry.

Adult-onset Still Disease Flare 5 Days Following Poly-l-lactic Acid Injection: A Cautionary Tale for Aesthetic Practice.

Secondary pulmonary alveolar proteinosis mimicking progression of interstitial lung disease during treatment for adult-onset still's disease: An autopsy case report.