Living with Feingold syndrome
A genetic condition affecting the fingers and toes, head size, face and learning, with two types.
Understanding Feingold syndrome
There are two types, based on genetic cause, with similar features that vary from person to person. Almost everyone has short second and fifth fingers. Common features include a small head, small jaw, narrow eyelid openings, and mild to moderate learning disabilities. Type 1 often includes a digestive blockage (gastrointestinal atresia). It is present from before or at birth.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Short fingers or toes (brachydactyly)
- Fifth fingers that curve inward
- Fused toes (syndactyly)
- Small head size (microcephaly)
- Small lower jaw (micrognathia)
- Learning problems or intellectual disability
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, brain and nervous system specialists, digestive system 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); Brain and nervous system specialists (neurologists); Digestive system specialists (gastroenterologists); 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 cause it. It is autosomal dominant, which means one changed copy of a gene is enough.
Also known as: brunner-winter syndrome; digital anomalies with short palpebral fissures and atresia of esophagus or duodenum; digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum; fglds; fs; microcephaly-digital anomalies-normal intelligence 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 Feingold syndrome.
Explore research for Feingold syndrome
Explore actively recruiting Feingold syndrome studies with HealthSpark.
Find actively recruiting studies for Feingold syndrome with HealthSpark. Share your city to explore research near you.
- Recruiting studies from ClinicalTrials.gov
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- Eligibility is confirmed by the study team
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Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.
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