Familial supernumerary nipples

Last reviewed

🖨 Print for my doctorAdvocacy Hub →
ORPHA:2456OMIM:163700Q83.3
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

Familial supernumerary nipples, also known as familial polythelia, is a congenital condition characterized by the presence of one or more additional nipples (accessory nipples) beyond the normal two. These extra nipples typically appear along the embryonic mammary ridge (milk line), which extends from the axilla (armpit) to the groin on both sides of the body. In the familial form, the condition clusters within families and follows a hereditary pattern. Supernumerary nipples may range from a small, barely noticeable mark resembling a mole to a more fully formed nipple, sometimes with surrounding areolar tissue. In rare cases, accessory breast tissue (polymastia) may also be present beneath the extra nipple. The condition primarily affects the skin and soft tissues of the chest and abdominal wall. Supernumerary nipples are usually asymptomatic and are often discovered incidentally during physical examination. They are generally considered a benign finding; however, in some cases, accessory nipples with underlying breast tissue may undergo hormonal changes (such as swelling or tenderness during puberty, menstruation, or pregnancy). Rarely, accessory breast tissue may be subject to the same pathological conditions as normal breast tissue, including benign tumors or, very rarely, malignancy. Some studies have suggested associations between supernumerary nipples and renal or urogenital anomalies, though this association remains debated in the medical literature. Treatment is generally not required unless there are cosmetic concerns or complications. Surgical excision can be performed for cosmetic reasons or if the accessory nipple causes discomfort or is associated with underlying glandular tissue that becomes symptomatic. Genetic counseling may be offered to affected families to discuss the hereditary nature of the condition and its generally benign prognosis.

Also known as:

Clinical phenotype terms— hover any for plain English:

Supernumerary nippleHP:0002558
Inheritance

Autosomal dominant

Passed on from just one parent; each child has about a 50% chance of inheriting it

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 Familial supernumerary nipples.

View clinical trials →

No actively recruiting trials found for Familial supernumerary nipples at this time.

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

Search ClinicalTrials.gov ↗Join the Familial supernumerary nipples community →

No specialists are currently listed for Familial supernumerary nipples.

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 Familial supernumerary nipples.

Search all travel grants →NORD Financial Assistance ↗

Community

Open Familial supernumerary nipplesForum →

No community posts yet. Be the first to share your experience with Familial supernumerary nipples.

Start the conversation →

Latest news about Familial supernumerary nipples

No recent news articles for Familial supernumerary nipples.

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.

Common questions about Familial supernumerary nipples

What is Familial supernumerary nipples?

Familial supernumerary nipples, also known as familial polythelia, is a congenital condition characterized by the presence of one or more additional nipples (accessory nipples) beyond the normal two. These extra nipples typically appear along the embryonic mammary ridge (milk line), which extends from the axilla (armpit) to the groin on both sides of the body. In the familial form, the condition clusters within families and follows a hereditary pattern. Supernumerary nipples may range from a small, barely noticeable mark resembling a mole to a more fully formed nipple, sometimes with surroundi

How is Familial supernumerary nipples inherited?

Familial supernumerary nipples follows a autosomal dominant inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Familial supernumerary nipples typically begin?

Typical onset of Familial supernumerary nipples is neonatal. Age of onset can vary across affected individuals.