Living with Symbrachydactyly of hands and feet
A rare condition in which fingers or toes are short, stiff, webbed, or missing.
Understanding Symbrachydactyly of hands and feet
Fingers and toes may be short, stiff, webbed, or missing, sometimes replaced with small stumps (nubbins) with nails. It can affect one or both sides of the body. Muscles, tendons, ligaments, and bones are affected, but there are no other limb differences. Signs are present from birth.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Short, stiff, or webbed fingers or toes
- Missing fingers or toes
- Small stumps with nails (nubbins)
- Small or missing thumb
- Differences in forearm bones
- Curved spine (scoliosis)
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. GARD doesn't list which gene or how it is inherited.
Also known as: de smet-fabry-fryns syndrome; frints de smet fabry fryns syndrome; symbrachydactyly of the hand and foot
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 Symbrachydactyly of hands and feet.
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