Feingold syndrome type 1

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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 June 2024

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Feingold syndrome type 1?

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