Oculodigitoesophagoduodenal syndrome

Common Name(s)

Oculodigitoesophagoduodenal syndrome, Feingold syndrome

Feingold syndrome is an autosomal dominant disorder characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. 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 in a minority of patients (summary by {23:Teszas et al., 2006}). Genetic Heterogeneity of Feingold Syndrome Feingold syndrome-2 (FGLDS2; {614326}) is caused by hemizygous deletion of the MIR17HG gene ({609415}) on chromosome 13q31.3.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Oculodigitoesophagoduodenal syndrome" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

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Research articles describe the outcome of a single study. They are the published results of original research.
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.