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Feingold syndrome
Disease 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) (see these terms). 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.
ORPHA:1305
Classification level: Disorder- Synonym(s):
- Brunner-Winter syndrome
- Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
- FGLDS
- FS
- MMT
- MODED syndrome
- Microcephaly-digital anomalies-normal intelligence syndrome
- Microcephaly-intellectual disability-tracheoesophageal fistula syndrome
- Microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome
- ODED syndrome
- Oculo-digito-esophageal-duodenal syndrome
- Prevalence: <1 / 1 000 000
- Inheritance: Autosomal dominant
- Age of onset: Neonatal
- ICD-10: Q87.8
- OMIM: 164280 614326
- UMLS: C0796068
- MeSH: -
- GARD: 8407
- MedDRA: -
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