Feingold syndrome

Feingold syndrome
Other namesOculodigitoesophagoduodenal syndrome
Feingold Syndrome is inherited in an autosomal dominant fashion.
SpecialtyMedical genetics 

Feingold syndrome (also called oculodigitoesophagoduodenal syndrome) is a rare autosomal dominant hereditary disorder. It is named after Murray Feingold, an American physician who first described the syndrome in 1975. Until 2003, at least 79 patients have been reported worldwide.

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