Living with Syndactyly-polydactyly-ear lobe syndrome
A rare genetic limb condition with webbed toes, an extra little finger, and ear lobe differences.
Understanding Syndactyly-polydactyly-ear lobe syndrome
The first and second toes are fully joined by skin. An extra finger on the little finger side ranges from a small nub to an almost complete finger. Ear lobes are shaped differently. X-rays may show differences along the inner edge of the foot. GARD notes no further descriptions in the literature since 1976.
Signs & symptoms
GARD doesn't list specific symptoms for this condition yet. The summary describes:
- Joined first and second toes
- Extra finger on the little finger side
- Ear lobe differences
- Foot bone differences on X-ray
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Specialists who may be involved include bone and joint specialists and genetic specialists.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
Care & treatment
- Care team
- Bone and joint specialists (orthopedists or orthopedic surgeons); Genetic specialists (geneticists)
- Expert care
- Ask about multidisciplinary care centers for rare conditions
- Treatment
- GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
- Research
- Clinical trials and observational studies may be options. See the research section below.
General information, not medical advice. Your care team makes the decisions.
Everyday life
Living with a rare condition is easier with support.
- Connect with rare disease patient organizations for support
- Keep notes on symptoms, changes and questions for appointments
- Ask about patient registries that help research
- Look into financial aid and travel resources for care visits
Quick facts
Changes in genes (variants) cause this condition. It is autosomal dominant, meaning one changed copy of a gene can cause it. GARD doesn't list which gene.
Also known as: spel syndrome; syndactyly-polydactyly-earlobe syndrome
Patient organizations
Rare-disease groups that can help
- Global GenesRare Diseases · United States
- National Organization for Rare DisordersRare Diseases · United States
- Genetic AllianceRare Diseases · United States
- RARE FoundationRare Diseases · United States
You are more than your diagnosis
Perspectives from people navigating life with Syndactyly-polydactyly-ear lobe syndrome.
Explore research for Syndactyly-polydactyly-ear lobe syndrome
Explore actively recruiting Syndactyly-polydactyly-ear lobe syndrome studies with HealthSpark.
Find actively recruiting studies for Syndactyly-polydactyly-ear lobe syndrome with HealthSpark. Share your city to explore research near you.
- Recruiting studies from ClinicalTrials.gov
- Share your city to look for research near you
- Eligibility is confirmed by the study team
Powered by HealthSpark, our AI chat helper
I can help you find recruiting Syndactyly-polydactyly-ear lobe syndrome studies. Enter a ZIP code, address or city below and I'll look within 50 miles.
Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.
Get Signals for Syndactyly-polydactyly-ear lobe syndrome
Stay in the loop with community stories and updates from medical researchers.
Create a living journal that talks back
HealthStory evolves private journaling with a living AI journal that talks back and asks thoughtful questions, helping you capture your Syndactyly-polydactyly-ear lobe syndrome experiences more deeply and prepare for better conversations with your doctors and care team.
Your journal is private. Sharing your story publicly is a separate choice, made with Share your story above.