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 Feingold syndrome hub →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
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.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Feingold syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Feingold syndrome from ClinicalTrials.gov on the hub.