Paediatria Croatica, Vol. 60 No. 2, 2016.
Case report
https://doi.org/10.13112/PC.2016.12
Diagnosis and surgical treatment of intestinal malrotation in a patient with Cornelia de Lange syndrome
Marija Vidaković
Sanda Huljev Frković
Vinka Barbarić Babić
Suzana Sršen Medančić
Marijan Frković
Davor Begović
Abstract
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.
Keywords
De Lange Syndrome; congenital abnormalities
Hrčak ID:
162372
URI
Publication date:
30.6.2016.
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