Viral myositis

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ORPHA:206991M60.0
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19Specialists8Treatment centers

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UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Viral myositis is an inflammatory muscle disease (classified under Orphanet code 206991; ICD-10: M60.0) caused by direct viral infection of skeletal muscle tissue or immune-mediated muscle inflammation triggered by a viral infection. It can affect individuals of any age but is particularly well-recognized in children, where it often presents as benign acute childhood myositis (BACM) following influenza or other viral infections. The condition primarily affects the musculoskeletal system, causing muscle pain (myalgia), tenderness, swelling, and weakness, most commonly in the calves and thighs. Patients may have difficulty walking or may refuse to bear weight. Elevated serum creatine kinase (CK) levels reflect muscle damage. Systemic symptoms such as fever, malaise, and upper respiratory symptoms often precede or accompany the muscle involvement. A wide range of viruses have been implicated, including influenza A and B (the most common cause in children), coxsackievirus, echovirus, HIV, HTLV-1, hepatitis B and C, Epstein-Barr virus, cytomegalovirus, and parainfluenza viruses. In most pediatric cases, particularly those associated with influenza, the condition is self-limiting and resolves within days to a week with supportive care including rest, hydration, and analgesics. However, in rare cases, viral myositis can progress to rhabdomyolysis, a severe breakdown of muscle tissue that can lead to acute kidney injury due to myoglobinuria, requiring urgent medical intervention including aggressive intravenous fluid resuscitation. In immunocompromised patients or those with HIV-associated myositis, the course may be more prolonged and require specific antiviral therapy or immunomodulatory treatment. There is no specific curative therapy for most forms of viral myositis; management is primarily supportive with monitoring of renal function and CK levels.

Inheritance

Sporadic

Usually appears on its own, not inherited from a parent

Age of Onset

Variable

Can begin at different ages, from infancy through adulthood

Orphanet ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Viral myositis.

View clinical trials →

No actively recruiting trials found for Viral myositis at this time.

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

Search ClinicalTrials.gov ↗Join the Viral myositis community →

Specialists

19 foundView all specialists →
EM
Edwin J Asturias, MD
AURORA, CO
Specialist
PI on 4 active trials
AK
Antonia-Therese Kietaibl
Specialist
1 Viral myositis publication
MF
Maria Fangmeyer-Binder
Specialist
1 Viral myositis publication
GG
Gabor Göndör
Specialist
1 Viral myositis publication
PB
Praveen Budde
ALEXANDRIA, LA
Specialist
1 Viral myositis publication
MG
Mindy Goh
TORRANCE, CA
Specialist
1 Viral myositis publication
CS
Charmi Shah
Specialist
1 Viral myositis publication
MD
Motahare A Delavar
Specialist
1 Viral myositis publication
HE
Hamidreza K Ebrahimi
Specialist
1 Viral myositis publication
NB
Nafise Borhani
Specialist
1 Viral myositis publication
PK
Pegah Karimian
Specialist
1 Viral myositis publication
FE
Fahimeh Ehsanipour
Specialist
1 Viral myositis publication
WS
William Stansbury
SHREVEPORT, LA
Specialist
1 Viral myositis publication
MP
Micah Pippin
ALEXANDRIA, LA
Specialist
1 Viral myositis publication
SJ
Shabahang Jafarnejad
Specialist
1 Viral myositis publication
SE
Somayeh Esmaeilian
Specialist
1 Viral myositis publication
SM
Suchitra Rao, MD
AURORA, CO
Specialist
PI on 1 active trial

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 Viral myositis.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Viral myositis

No recent news articles for Viral myositis.

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

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

Common questions about Viral myositis

What is Viral myositis?

Viral myositis is an inflammatory muscle disease (classified under Orphanet code 206991; ICD-10: M60.0) caused by direct viral infection of skeletal muscle tissue or immune-mediated muscle inflammation triggered by a viral infection. It can affect individuals of any age but is particularly well-recognized in children, where it often presents as benign acute childhood myositis (BACM) following influenza or other viral infections. The condition primarily affects the musculoskeletal system, causing muscle pain (myalgia), tenderness, swelling, and weakness, most commonly in the calves and thighs.

How is Viral myositis inherited?

Viral myositis follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

Which specialists treat Viral myositis?

19 specialists and care centers treating Viral myositis are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.