Feingold syndrome

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, 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 oesophagus or duodenum

0 clinical trials for this condition and its sub-types, 0 tagged with Feingold syndrome itself.