Crossed polysyndactyly

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ORPHA:2935OMIM:175690Q70.4
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5Specialists8Treatment centers

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

Crossed polysyndactyly is a very rare birth defect that affects the fingers and toes. In this condition, a person is born with extra fingers (polydactyly) on one hand or both hands and fused or webbed toes (syndactyly) on one or both feet, or vice versa — meaning the type of abnormality 'crosses' between the hands and feet rather than being the same in both. For example, a person might have extra fingers on their hands but webbed toes on their feet. The condition is present at birth and is typically noticed right away during a newborn examination. Crossed polysyndactyly can vary in severity. Some individuals may have mild webbing between toes or a small extra finger, while others may have more complex hand or foot differences that affect function. The condition primarily affects the structure of the hands and feet and does not usually involve other organ systems or intellectual development. Treatment is mainly surgical. Depending on the severity, surgery may be performed to remove extra fingers, separate fused toes, or improve the function and appearance of the hands and feet. Occupational therapy and physical therapy may also be recommended after surgery to help with hand function and mobility. With appropriate treatment, most individuals with crossed polysyndactyly can lead normal, active lives. Early evaluation by a hand surgeon or orthopedic specialist experienced in limb differences is important for planning the best approach to care.

Key symptoms:

Extra fingers on one or both handsWebbed or fused toes on one or both feetExtra toes on one or both feetWebbed or fused fingers on one or both handsDifferent types of hand and foot abnormalities on opposite limbsDifficulty gripping or grasping objects if hands are affectedDifficulty with walking or shoe fitting if feet are affectedAbnormal appearance of fingers or toes

Clinical phenotype terms (11)— hover any for plain English
Abnormality of the philtrumHP:0000288
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 Crossed polysyndactyly.

View clinical trials →

No actively recruiting trials found for Crossed polysyndactyly at this time.

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

Search ClinicalTrials.gov ↗Join the Crossed polysyndactyly community →

Specialists

5 foundView all specialists →
GT
Gianluca Tamaro
Specialist
1 Crossed polysyndactyly publication
FB
Francesco Baldo
Specialist
1 Crossed polysyndactyly publication
BS
Beatrice Spedicati
Specialist
1 Crossed polysyndactyly publication
AT
Andrea Taddio
Specialist
1 Crossed polysyndactyly publication
FF
Flavio Faletra
Specialist
1 Crossed polysyndactyly publication

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 Crossed polysyndactyly.

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Community

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Latest news about Crossed polysyndactyly

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

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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.How severe is my child's condition, and which fingers or toes are affected?,When is the best time to have corrective surgery?,How many surgeries might be needed, and what are the expected outcomes?,Will my child need occupational or physical therapy after surgery?,Is genetic testing recommended for our family?,What is the chance that future children could have the same condition?,Are there any long-term complications we should watch for?

Common questions about Crossed polysyndactyly

What is Crossed polysyndactyly?

Crossed polysyndactyly is a very rare birth defect that affects the fingers and toes. In this condition, a person is born with extra fingers (polydactyly) on one hand or both hands and fused or webbed toes (syndactyly) on one or both feet, or vice versa — meaning the type of abnormality 'crosses' between the hands and feet rather than being the same in both. For example, a person might have extra fingers on their hands but webbed toes on their feet. The condition is present at birth and is typically noticed right away during a newborn examination. Crossed polysyndactyly can vary in severity.

How is Crossed polysyndactyly inherited?

Crossed polysyndactyly follows a autosomal dominant inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Crossed polysyndactyly typically begin?

Typical onset of Crossed polysyndactyly is neonatal. Age of onset can vary across affected individuals.

Which specialists treat Crossed polysyndactyly?

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