OBSOLETE: Hyperphalangy, unilateral

Last reviewed

🖨 Print for my doctorAdvocacy Hub →
ORPHA:295140
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

Hyperphalangy, unilateral is an extremely rare skeletal condition in which one or more fingers or toes on one side of the body have extra small bones (called phalanges) within the digits. Normally, fingers have a set number of small bones, but in this condition, there are additional ones, which can change the shape or length of the affected digits. The term 'unilateral' means it affects only one side of the body — either the right or the left hand or foot, but not both. This condition is listed as 'OBSOLETE' in the Orphanet classification, meaning it may have been reclassified, merged with another diagnosis, or is no longer considered a distinct clinical entity in current medical terminology. Because of this obsolete status, very little specific clinical information, research, or treatment guidelines exist under this exact name. If you or your child has been given this diagnosis, it is important to work with a clinical geneticist or orthopedic specialist who can help determine whether a more current diagnosis applies. Treatment, if needed, is typically focused on improving hand or foot function and may include physical therapy or, in some cases, surgery. The condition is generally not life-threatening and primarily affects the structure and function of the involved digits.

Also known as:

Key symptoms:

Extra bones in the fingers or toes on one side of the bodyUnusually long or oddly shaped fingers or toesStiffness in the affected digitsDifficulty gripping or grasping objectsVisible difference in finger or toe length between hands or feetLimited range of motion in affected digits

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: Hyperphalangy, unilateral.

View clinical trials →

No actively recruiting trials found for OBSOLETE: Hyperphalangy, unilateral at this time.

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

Search ClinicalTrials.gov ↗Join the OBSOLETE: Hyperphalangy, unilateral community →

No specialists are currently listed for OBSOLETE: Hyperphalangy, 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: Hyperphalangy, unilateral.

Search all travel grants →NORD Financial Assistance ↗

Community

Open OBSOLETE: Hyperphalangy, unilateralForum →

No community posts yet. Be the first to share your experience with OBSOLETE: Hyperphalangy, unilateral.

Start the conversation →

Latest news about OBSOLETE: Hyperphalangy, unilateral

No recent news articles for OBSOLETE: Hyperphalangy, 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.Is this diagnosis still considered current, or has it been reclassified under a different name?,Could this be part of a broader genetic syndrome?,Should my child have genetic testing?,Will the extra bones cause any functional problems as my child grows?,Is surgery recommended, or can we manage this with therapy alone?,How often should we follow up with imaging or specialist visits?,Are there any related conditions we should screen for?

Common questions about OBSOLETE: Hyperphalangy, unilateral

What is OBSOLETE: Hyperphalangy, unilateral?

Hyperphalangy, unilateral is an extremely rare skeletal condition in which one or more fingers or toes on one side of the body have extra small bones (called phalanges) within the digits. Normally, fingers have a set number of small bones, but in this condition, there are additional ones, which can change the shape or length of the affected digits. The term 'unilateral' means it affects only one side of the body — either the right or the left hand or foot, but not both. This condition is listed as 'OBSOLETE' in the Orphanet classification, meaning it may have been reclassified, merged with ano

At what age does OBSOLETE: Hyperphalangy, unilateral typically begin?

Typical onset of OBSOLETE: Hyperphalangy, unilateral is neonatal. Age of onset can vary across affected individuals.