Diagnosis and surgical treatment of intestinal malrotation in a patient with Cornelia de Lange syndrome
DOI:
https://doi.org/10.13112/PC.2016.12Keywords:
de Lange Syndrome, congenital abnormalitiesAbstract
We report on a female infant with phenotypic characteristics of Cornelia de Lange syndrome and associated, successfully surgically treated, intestinal malrotation. The purpose of this report is to point out that intestinal malrotation, as a rare element of Cornelia de Lange syndrome, should not be left out on the diff erential diagnosis of gastrointestinal symptoms in these patients.
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