/Feingold syndrome

Feingold syndrome

Rare Disease

MONDO:0015267

Also Known As

Brunner-Winter syndromeFGLDSFSMMTMODED syndromeODED syndromedigital anomalies with short palpebral fissures and atresia of esophagus or duodenumdigital anomalies with short palpebral fissures and atresia of oesophagus or duodenummicrocephaly-digital anomalies-normal intelligence syndromemicrocephaly-intellectual disability-tracheoesophageal fistula syndromemicrocephaly-oculo-digito-esophageal-duodenal syndromemicrocephaly-oculo-digito-esophageal-duodenal syndrome syndromeoculo-digito-esophageal-duodenal syndromedigital anomalies with short palpebral fissures and atresia of esophagus, or duodenum

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.