Feingold syndrome type 1
Feingold syndrome type 1
Definition
Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.
Also known as Brunner-Winter syndrome type 1, digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1, digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1, Feingold syndrome caused by mutation in MYCN, Feingold syndrome type 1, FGLDS1, FS1, 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, MMT type 1, MODED syndrome type 1, MYCN Feingold syndrome, oculo-digito-esophageal-duodenal syndrome type 1, ODED syndrome type 1 — per MONDO