Eyebrow duplication-syndactyly syndrome

Last reviewed

🖨 Print for my doctorAdvocacy Hub →
ORPHA:3172OMIM:227210Q87.8
Who is this for?
Show terms as
8Treatment centers

Where are you in your journey?

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

Overview

Eyebrow duplication-syndactyly syndrome is an extremely rare genetic condition that is present from birth. As the name suggests, the two main features of this syndrome are duplication (doubling) of the eyebrows and syndactyly, which means that some fingers or toes are fused or webbed together. The eyebrow duplication can range from a thickened, bushy appearance to what looks like two distinct rows of eyebrow hair. The syndactyly typically involves the soft tissue between fingers or toes, though in some cases the bones may also be joined. Because this condition is so rare, with only a handful of cases described in the medical literature, the full range of possible symptoms and the underlying genetic cause are not yet well understood. There is no cure for this syndrome, and treatment focuses on managing the individual features. Surgery may be considered to separate fused fingers or toes and improve hand or foot function. Cosmetic approaches can address the eyebrow duplication if desired. Affected individuals should be followed by a team of specialists to monitor for any additional features that may be associated with the condition. The long-term outlook depends on the severity of the features and how well they respond to treatment.

Key symptoms:

Double or duplicated eyebrowsThickened or unusually bushy eyebrowsWebbed or fused fingersWebbed or fused toesUnusual facial appearancePossible limb abnormalities

Inheritance

Variable

Can be inherited in different ways depending on the underlying gene

Age of Onset

Neonatal

Begins at or shortly after birth (first 4 weeks)

Orphanet ↗OMIM ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Eyebrow duplication-syndactyly syndrome.

View clinical trials →

No actively recruiting trials found for Eyebrow duplication-syndactyly syndrome at this time.

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

Search ClinicalTrials.gov ↗Join the Eyebrow duplication-syndactyly syndrome community →

No specialists are currently listed for Eyebrow duplication-syndactyly syndrome.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

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 Eyebrow duplication-syndactyly syndrome.

Search all travel grants →NORD Financial Assistance ↗

Community

Open Eyebrow duplication-syndactyly syndromeForum →

No community posts yet. Be the first to share your experience with Eyebrow duplication-syndactyly syndrome.

Start the conversation →

Latest news about Eyebrow duplication-syndactyly syndrome

No recent news articles for Eyebrow duplication-syndactyly syndrome.

Follow this condition to be notified when news becomes available.

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.What is the best age for my child to have surgery to separate fused fingers or toes?,Are there any other health problems we should watch for with this condition?,Is genetic testing available to find the cause, and would it help our family?,What are the risks and expected outcomes of syndactyly release surgery?,Should we see any other specialists?,What are the chances that future children could also be affected?,Are there any clinical studies or research programs we could participate in?

Common questions about Eyebrow duplication-syndactyly syndrome

What is Eyebrow duplication-syndactyly syndrome?

Eyebrow duplication-syndactyly syndrome is an extremely rare genetic condition that is present from birth. As the name suggests, the two main features of this syndrome are duplication (doubling) of the eyebrows and syndactyly, which means that some fingers or toes are fused or webbed together. The eyebrow duplication can range from a thickened, bushy appearance to what looks like two distinct rows of eyebrow hair. The syndactyly typically involves the soft tissue between fingers or toes, though in some cases the bones may also be joined. Because this condition is so rare, with only a handful o

At what age does Eyebrow duplication-syndactyly syndrome typically begin?

Typical onset of Eyebrow duplication-syndactyly syndrome is neonatal. Age of onset can vary across affected individuals.