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Afr J Paediatr Surg ; 13(1): 47-9, 2016.
Article in English | MEDLINE | ID: mdl-27251525

ABSTRACT

Congenital diaphragmatic hernia (CDH) is a common developmental anomaly that usually presents in the neonatal period. It is known to be associated with cardiac, renal, genital and chromosomal anomalies. Late presentation of CDH (beyond 1-month of age) is seen in 13% of the cases. Malrotation is reported in 42% of CDH cases. We report a case of a 3-month-old infant with concurrent CDH, Meckel's diverticulum and malrotation. This is the first case report of such an association in an infant.


Subject(s)
Digestive System Abnormalities/surgery , Hernias, Diaphragmatic, Congenital/surgery , Intestinal Volvulus/surgery , Meckel Diverticulum/surgery , Digestive System Abnormalities/complications , Digestive System Abnormalities/diagnostic imaging , Hernias, Diaphragmatic, Congenital/complications , Hernias, Diaphragmatic, Congenital/diagnostic imaging , Humans , Infant , Intestinal Volvulus/complications , Intestinal Volvulus/diagnostic imaging , Male , Meckel Diverticulum/complications , Meckel Diverticulum/diagnostic imaging
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