You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Feingold syndrome type 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Feingold syndrome type 1 hub →Feingold syndrome type 1 is a rare condition. Also known as Brunner-Winter syndrome type 1, Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1, FGLDS1, FS1, MMT type 1, MODED syndrome type 1, Microcephaly-digital anomalies-normal intelligence syndrome type 1, Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Feingold syndrome type 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:391641 · OMIM 164280 · ICD-10 Q87.8 · GARD 0017624
Start by learning the basics from an authoritative source, find a specialist or center that sees Feingold syndrome type 1, 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 type 1, filtered to your area.
Tomeko shows live, recruiting studies for Feingold syndrome type 1 from ClinicalTrials.gov on the hub.