Argyria

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15Specialists8Treatment centers

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

Argyria (also called argyrosis or silver poisoning) is a rare condition caused by too much silver building up in the body over time. Silver can enter the body through swallowing silver-containing supplements or medicines, breathing in silver dust or fumes at work, or having silver-containing wound dressings used for long periods. Once silver gets into the skin and other tissues, it causes a permanent blue-gray or slate-gray discoloration. The skin color change is most noticeable on areas exposed to sunlight, such as the face, hands, and neck, but it can affect the entire body including the eyes, nails, and internal organs. The most well-known symptom is the striking skin color change, which is permanent and does not go away even after stopping silver exposure. Beyond the cosmetic effects, argyria is generally not life-threatening, but it can cause significant emotional distress and social challenges. Some people also experience sensitivity to sunlight. The condition is diagnosed mainly by looking at the skin and confirming silver deposits through a skin biopsy. There is no proven cure or treatment that reverses the skin discoloration. Management focuses on stopping further silver exposure and using cosmetic cover-up products to help with appearance. Prevention is the most important strategy, which means avoiding unnecessary silver supplements and being careful in workplaces where silver exposure is possible.

Also known as:

Key symptoms:

Permanent blue-gray or slate-gray skin color, especially on sun-exposed areasGrayish discoloration of the whites of the eyes (sclerae)Darkening of the nailsGrayish color inside the mouth and gumsIncreased sensitivity to sunlightDiscoloration of internal organs (found on imaging or autopsy, usually no symptoms)Emotional distress or anxiety about appearanceSocial withdrawal due to visible skin changes

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 Argyria.

View clinical trials →

No actively recruiting trials found for Argyria at this time.

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

Search ClinicalTrials.gov ↗Join the Argyria community →

Specialists

15 foundView all specialists →
PA
Phyu P Aung
HOUSTON, TX
Specialist
1 Argyria publication
VP
Victor G Prieto
SAN ANTONIO, TX
Specialist
1 Argyria publication
CT
Carlos A Torres-Cabala
Specialist
1 Argyria publication
TL
Tin Yan Lee
Specialist
1 Argyria publication
WL
Wan Hang Lau
MONTEREY PARK, CA
Specialist
1 Argyria publication
LM
Luís Mota
Specialist
1 Argyria publication
RD
Ricardo Jorge Dinis-Oliveira
Specialist
1 Argyria publication
PG
Pavandeep Gill
HOUSTON, TX
Specialist
1 Argyria publication
KR
Kristen Richards
Specialist
1 Argyria publication
WC
Woo Cheal Cho
Specialist
1 Argyria publication
PN
Priyadharsini Nagarajan
HOUSTON, TX
Specialist
1 Argyria publication
DI
Doina Ivan
HOUSTON, TX
Specialist
1 Argyria publication
JC
Jonathan L Curry
Specialist
1 Argyria publication
AB
Adriano Bonura
Specialist
1 Argyria publication
MS
Marlene Saßmannshausen
Specialist
2 Argyria publications

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 Argyria.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Argyria

No recent news articles for Argyria.

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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.Is my skin discoloration definitely argyria, and how was that confirmed?,Will the skin color change get worse over time, and can anything stop it from progressing?,Are there any treatments, such as laser therapy, that might reduce the discoloration in my case?,What sun protection measures do you recommend for me specifically?,Are there any health risks beyond the skin changes that I should be aware of?,Can you refer me to a mental health professional or support group to help me cope with the appearance changes?,Are there any clinical trials or new treatments being studied for argyria?

Common questions about Argyria

What is Argyria?

Argyria (also called argyrosis or silver poisoning) is a rare condition caused by too much silver building up in the body over time. Silver can enter the body through swallowing silver-containing supplements or medicines, breathing in silver dust or fumes at work, or having silver-containing wound dressings used for long periods. Once silver gets into the skin and other tissues, it causes a permanent blue-gray or slate-gray discoloration. The skin color change is most noticeable on areas exposed to sunlight, such as the face, hands, and neck, but it can affect the entire body including the eye

How is Argyria inherited?

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

Which specialists treat Argyria?

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