OBSOLETE: Postaxial polydactyly type B, unilateral

Last reviewed

🖨 Print for my doctorAdvocacy Hub →
ORPHA:295167
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

Postaxial polydactyly type B, unilateral, is a condition where a baby is born with an extra small finger or toe on the outer side (the side of the pinky finger or little toe) of one hand or one foot. The term 'postaxial' means the extra digit is on the outer edge of the hand or foot. In type B, the extra digit is usually small, soft, and poorly formed — often described as a small nub or skin tag rather than a fully developed finger or toe. The word 'unilateral' means it affects only one side of the body. This entry is now labeled as 'OBSOLETE' in medical classification systems, meaning it has been merged into a broader category of postaxial polydactyly for classification purposes. However, the condition itself still occurs and is one of the most common congenital limb differences seen at birth. Treatment is usually straightforward. In many cases, the small extra digit can be removed shortly after birth by tying it off with a suture (if it is a small skin tag) or through a minor surgical procedure. The condition typically does not affect a child's overall health, development, or life expectancy. It can occur as an isolated finding or sometimes as part of a broader genetic syndrome, so a medical evaluation is recommended to rule out other associated conditions.

Key symptoms:

Extra small finger or toe on the outer side of the hand or footSmall skin tag or nub near the pinky finger or little toeSoft, poorly formed extra digitExtra digit present on only one hand or one footThe extra digit may or may not have a small nailThe extra digit may be attached by a thin stalk of skin

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 ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for OBSOLETE: Postaxial polydactyly type B, unilateral.

View clinical trials →

No actively recruiting trials found for OBSOLETE: Postaxial polydactyly type B, unilateral at this time.

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

Search ClinicalTrials.gov ↗Join the OBSOLETE: Postaxial polydactyly type B, unilateral community →

No specialists are currently listed for OBSOLETE: Postaxial polydactyly type B, unilateral.

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 OBSOLETE: Postaxial polydactyly type B, unilateral.

Search all travel grants →NORD Financial Assistance ↗

Community

Open OBSOLETE: Postaxial polydactyly type B, unilateralForum →

No community posts yet. Be the first to share your experience with OBSOLETE: Postaxial polydactyly type B, unilateral.

Start the conversation →

Latest news about OBSOLETE: Postaxial polydactyly type B, unilateral

No recent news articles for OBSOLETE: Postaxial polydactyly type B, unilateral.

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.Does my child's extra digit contain any bone, and how does that affect treatment?,Is this an isolated finding, or could it be part of a genetic syndrome?,What is the best method for removing the extra digit in my child's case?,When is the ideal time to have the extra digit removed?,Should we see a geneticist or have genetic testing done?,What is the chance that future children could also have this condition?,What should I watch for after the extra digit is removed?

Common questions about OBSOLETE: Postaxial polydactyly type B, unilateral

What is OBSOLETE: Postaxial polydactyly type B, unilateral?

Postaxial polydactyly type B, unilateral, is a condition where a baby is born with an extra small finger or toe on the outer side (the side of the pinky finger or little toe) of one hand or one foot. The term 'postaxial' means the extra digit is on the outer edge of the hand or foot. In type B, the extra digit is usually small, soft, and poorly formed — often described as a small nub or skin tag rather than a fully developed finger or toe. The word 'unilateral' means it affects only one side of the body. This entry is now labeled as 'OBSOLETE' in medical classification systems, meaning it has

At what age does OBSOLETE: Postaxial polydactyly type B, unilateral typically begin?

Typical onset of OBSOLETE: Postaxial polydactyly type B, unilateral is neonatal. Age of onset can vary across affected individuals.