Feingold syndrome type 1
Synonyms: 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 | Microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1 | ODED syndrome type 1 | Oculo-digito-esophageal-duodenal syndrome type 1
A rare genetic congenital malformation syndrome characterized by digital anomalies (shortening of the 2nd and 5th middle phalanx of the hand clinodactyly of the 5th finger syndactyly of toes 2-3 and/or 4-5 thumb hypoplasia) microcephaly facial dysmorphism (short palpebral fissures and micrognathia) gastrointestinal atresia (primarily esophageal and/or duodenal) and mild-to-moderate learning disability.
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 April 2024
Newly diagnosed with
Feingold syndrome type 1?
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Advocacy Organizations
COMBINEDBrain Inc
COMBINEDBrain is a consortium for outcome measures and biomarkers for neurodevelopmental disorders. We are collaborating to cure rare, non-verbal brain disorders.
DDX3X Foundation
Our mission is to connect families, resources, and the medical community to advance research for a treatment or cure to DDX3X Syndrome. Our ultimate goal is to accelerate brain function in individuals affected by DDX3X Syndrome through advances in cell and gene therapy and pharmaceuticals.
Help Hope Live
Help Hope Live assists individuals living with catastrophic injuries and illnesses to fundraise toward their medical expenses and related costs.
Moonshots for Unicorns
Curing single-gene disorders
Project CASK
To fund research for treatment and/or a cure for CASK Gene Disorder
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.