Brunner-Winter syndrome type 1FGLDS1FS1Feingold syndrome caused by mutation in MYCNFeingold syndrome type 1MMT type 1MODED syndrome type 1MYCN Feingold syndromeODED syndrome type 1digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1microcephaly-digital anomalies-normal intelligence syndrome type 1microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1oculo-digito-esophageal-duodenal syndrome type 1Feingold syndromeFeingold syndrome 1Mmt syndromeOded syndromedigital anomalies with short palpebral fissures and atresia of esophagus or duodenumdigital anomalies with short palpebral fissures and atresia of oesophagus or duodenummicrocephaly and digital abnormalities with normal intelligencemicrocephaly, intellectual disability, and tracheoesophageal fistula syndromemicrocephaly, mental retardation, and tracheoesophageal fistula syndromemicrocephaly-oculo-digito-esophageal-duodenal syndromeoculodigitoesophagoduodenal syndrome
Definition
Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.
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