Feingold syndrome
Feingold syndrome
Definition
Feingold syndrome (FS), also known as oculo-digito-esophageal-duodenal (ODED) syndrome, is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies and is comprised of two subtypes: FS type 1 (FS1) and FS type 2 (FS2). FS1 is by far the most common form while FS2 has only been reported in 3 patients and has the same clinical characteristics as FS1, apart from the absence of gastrointestinal atresia and short palpebral fissures.
Also known as Brunner-Winter syndrome, digital anomalies with short palpebral fissures and atresia of esophagus or duodenum, digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum, FGLDS, FS, microcephaly-digital anomalies-normal intelligence syndrome, microcephaly-intellectual disability-tracheoesophageal fistula syndrome, microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome, MMT, MODED syndrome, oculo-digito-esophageal-duodenal syndrome, ODED syndrome — per MONDO