Just diagnosed with Feingold syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Feingold syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Feingold syndrome hub →Overview
Feingold syndrome is a rare condition. Also known as Brunner-Winter syndrome, Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum, FGLDS, FS, MMT, MODED syndrome, Microcephaly-digital anomalies-normal intelligence syndrome, Microcephaly-intellectual disability-tracheoesophageal fistula syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Feingold syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1305 · OMIM 164280, 614326 · ICD-10 Q87.8 · GARD 0008407
Find care for Feingold syndrome
Authoritative references for Feingold syndrome
Research & market landscape for Feingold syndrome
Following Feingold syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Feingold syndrome — the real-world landscape behind the condition, in one place.
- Latest Feingold syndrome research on PubMed ↗
- Recruiting Feingold syndrome trials on ClinicalTrials.gov ↗
- Explore the Feingold syndrome research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Feingold syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Feingold syndrome?
Feingold syndrome is a rare condition. Also known as Brunner-Winter syndrome, Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum, FGLDS, FS, MMT, MODED syndrome, Microcephaly-digital anomalies-normal intelligence syndrome, Microcephaly-intellectual disability-tracheoesophageal fistula syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Feingold syndrome together in one place.
What are the symptoms of Feingold syndrome?
Symptoms of Feingold syndrome vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Feingold syndrome.
How is Feingold syndrome treated?
Treatment for Feingold syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Feingold syndrome, and review current options with them.
What causes Feingold syndrome — is it genetic?
The cause and inheritance of Feingold syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Feingold syndrome can explain what it means for you and your family.
I was just diagnosed with Feingold syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Feingold syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Feingold syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Feingold syndrome, filtered to your area.
Are there clinical trials for Feingold syndrome?
Tomeko shows live, recruiting studies for Feingold syndrome from ClinicalTrials.gov on the hub.
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