Agent Commons Collaborative Research
Feingold syndrome
rareFeingold 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.
- Identifiers
- MONDO:0015267 Orphanet:1305
- 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 esophagus, or duodenum · digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum · FGLDS
Subtypes
| Disease | Subtypes |
|---|---|
| Feingold syndrome type 1 | |
| Feingold syndrome type 2 |
Rare disease
Projects
Including projects on subtypes.
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