Feingold syndrome

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Synonyms: 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 | Microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome | ODED syndrome | Oculo-digito-esophageal-duodenal syndrome

A rare genetic congenital malformation syndrome characterized by microcephaly short stature and numerous digital anomalies (brachymesophanlangy fifth finger clinodactyly syndactyly of toes and hypoplastic thumbs) mild learning deficit and short palpebral fissures. The two subtypes are clinically distinguished by the presence (type 1) or absence (type 2) gastrointestinal atresia.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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Feingold syndrome?

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Advocacy Organizations

Help Hope Live

Help Hope Live supports community-based fundraising for people with unmet medical expenses and related costs due to cell and organ transplants or catastrophic injuries and illnesses. These efforts play a critical role in helping clients access the care and equipment they need to heal, live, and thrive. Unlock a powerful and safe way to raise funds for medical needs with Help Hope Live. They provide one-on-one fundraising guidance, a customizable Campaign Page, bill pay support, and additional benefits based on their 501(c)(3) nonprofit status.

Project CASK

VISION Project CASK believes in a world free of the life limitations and debilitating effects of CASK gene disorders. ​MISSION To accelerate breakthroughs in research to develop treatments and a cure for CASK gene disorders. ​VALUES Collaboration. Transparency. Urgency.

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Clinical Trials

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