You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Feingold syndrome type 2, look for clinical trials, and connect with others living with it — all in one place.
Open the full Feingold syndrome type 2 hub →Feingold syndrome type 2 is a rare condition. Also known as Brachydactyly-short stature-microcephaly syndrome, Brunner-Winter syndrome type 2, FGLDS2, FS2, MMT type 2, Microcephaly-digital anomalies-normal intelligence syndrome type 2, Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2. Tomeko brings together the specialists, research, clinical trials, treatments and community for Feingold syndrome type 2 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:391646 · OMIM 614326 · ICD-10 Q87.8 · GARD 0017625
Start by learning the basics from an authoritative source, find a specialist or center that sees Feingold syndrome type 2, 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 2, filtered to your area.
Tomeko shows live, recruiting studies for Feingold syndrome type 2 from ClinicalTrials.gov on the hub.