Orphanet: Feingold syndrome
x

Search for a rare disease

* (*) mandatory field

Other search option(s)

Suggest an update

(*) Required fields.

Attention

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

Feingold syndrome

Disease definition

A rare genetic, congenital malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies (brachymesophanlangy, fifth finger clinodactyly, syndactyly of toes and hypoplastic thumbs), mild learning deficit and short palpebral fissures. The two subtypes are clinically distinguished by the presence (type 1) or absence (type 2) gastrointestinal atresia.

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: -

Detailed information

Professionals

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.