Disease - Feingold syndrome 1
Definition
A syndrome characterized by variable combinations of esophageal and duodenal atresias, microcephaly, learning disability, mental retardation, and limb malformations. Hand and foot abnormalities may include hypoplastic thumbs, clinodactyly of second and fifth fingers, syndactyly (characteristically between second and third and fourth and fifth toes), and shortened or absent middle phalanges. Cardiac and renal malformations, vertebral anomalies, and deafness have also been described.
Acronym
FGLDS1
Synonyms
Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
Microcephaly and digital abnormalities with normal intelligence
Microcephaly mental retardation and tracheoesophageal fistula syndrome
Microcephaly-oculo-digito-esophageal-duodenal syndrome
MMT syndrome
MODED
Oculodigitoesophagoduodenal syndrome
ODED
Microcephaly and digital abnormalities with normal intelligence
Microcephaly mental retardation and tracheoesophageal fistula syndrome
Microcephaly-oculo-digito-esophageal-duodenal syndrome
MMT syndrome
MODED
Oculodigitoesophagoduodenal syndrome
ODED
Disclaimer
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. Our staff consists of biologists and biochemists that are not trained to give medical advice.
