Nocardiosis

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ORPHA:31204A43.0A43.1A43.8
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7Specialists8Treatment centers

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

Nocardiosis is a rare bacterial infection caused by bacteria called Nocardia. These bacteria are found naturally in soil, water, and decaying plant matter around the world. Most healthy people who come into contact with Nocardia never get sick. However, people with weakened immune systems — such as those with HIV/AIDS, organ transplants, cancer, or long-term steroid use — are much more vulnerable to developing this infection. Nocardia bacteria can enter the body through the lungs when a person breathes in contaminated dust or soil particles. From there, the infection can spread through the bloodstream to other parts of the body, most commonly the brain, skin, and soft tissues. When the infection stays in the lungs, it causes symptoms similar to pneumonia. When it spreads to the brain, it can cause abscesses — pockets of infection — that are very serious. Skin infections can happen when bacteria enter through a cut or wound. Nocardiosis is treated with antibiotics, usually for a long period of time — often six months to a year or more, especially if the brain is involved. The most commonly used antibiotic is trimethoprim-sulfamethoxazole (TMP-SMX), though other antibiotics like imipenem, amikacin, or linezolid may also be used. With proper treatment, many people recover, but the disease can be life-threatening if not caught and treated early, particularly in people with severely weakened immune systems.

Key symptoms:

Persistent cough that does not go awayFever and chillsChest pain when breathingShortness of breathFatigue and general weaknessNight sweatsUnexplained weight lossHeadachesConfusion or changes in thinkingSkin sores or lumps that may drain fluidSwollen lymph nodesMuscle weakness or difficulty movingSeizures (if the brain is affected)

Clinical phenotype terms (50)— hover any for plain English
Productive coughHP:0031245BacteremiaHP:0031864Abnormal sputumHP:0032016DacryocystitisHP:0000620EmphysemaHP:0002097PleuritisHP:0002102
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 Nocardiosis.

View clinical trials →

No actively recruiting trials found for Nocardiosis at this time.

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

Search ClinicalTrials.gov ↗Join the Nocardiosis community →

Specialists

7 foundView all specialists →
AP
Ahmed Fahal, Prof
Specialist
PI on 1 active trial
DP
Doudou Sow, PhD
Specialist
PI on 1 active trial
SM
Shivaprakash M Rudramurthy, M.D
Specialist
PI on 1 active trial
MP
Mohamed Osman, PhD
Specialist
PI on 1 active trial
VD
Vishwananath gella, DM
Specialist
PI on 1 active trial
DM
Daniel E Barquero Orias, MD
Specialist
PI on 1 active trial
MG
Margaux MD Garzaro
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 Nocardiosis.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Nocardiosis

No recent news articles for Nocardiosis.

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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.

Questions for your doctor

Bring these to your next appointment

  • Q1.Which type of Nocardia bacteria do I have, and does that affect which antibiotic I should take?,How long will I need to take antibiotics, and what side effects should I watch out for?,Do I need any imaging tests like a CT scan of my brain to check if the infection has spread?,What signs should prompt me to go to the emergency room right away?,Will my immune system condition make it harder to treat this infection, and do I need to change any of my other medications?,How will we know the treatment is working, and how often will I need follow-up tests?,Is there a risk that the infection will come back, and if so, what can be done to prevent that?

Common questions about Nocardiosis

What is Nocardiosis?

Nocardiosis is a rare bacterial infection caused by bacteria called Nocardia. These bacteria are found naturally in soil, water, and decaying plant matter around the world. Most healthy people who come into contact with Nocardia never get sick. However, people with weakened immune systems — such as those with HIV/AIDS, organ transplants, cancer, or long-term steroid use — are much more vulnerable to developing this infection. Nocardia bacteria can enter the body through the lungs when a person breathes in contaminated dust or soil particles. From there, the infection can spread through the bl

How is Nocardiosis inherited?

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

Which specialists treat Nocardiosis?

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