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oculodigitoesophagoduodenal syndrome (Feingold syndrome)
Pathology:
- variable combinations of esophageal & duodenal atresias, microcephaly, learning disability & limb malformations
- cardiac & renal malformations, vertebral anomalies, & deafness have also been described
Genetics:
- associated with defects in N-myc
General
genetic syndrome (multisystem disorder)
References
UniProt :accession P04198