Feingold syndrome

Disease Overview

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.

Synonyms

• Brunner-Winter syndrome
• FGLDS
• FS
• MMT
• MODED syndrome
• ODED syndrome
• digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
• digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
• digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum
• microcephaly-digital anomalies-normal intelligence syndrome
• microcephaly-intellectual disability-tracheoesophageal fistula syndrome
• microcephaly-oculo-digito-esophageal-duodenal syndrome
• microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome
• oculo-digito-esophageal-duodenal syndromeBrunner-Winter syndrome
• FGLDS
• FS
• MMT
• MODED syndrome
• ODED syndrome
• digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
• digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
• digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum
• microcephaly-digital anomalies-normal intelligence syndrome
• microcephaly-intellectual disability-tracheoesophageal fistula syndrome
• microcephaly-oculo-digito-esophageal-duodenal syndrome
• microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome
• oculo-digito-esophageal-duodenal syndrome