Article ID Journal Published Year Pages File Type
4161280 Journal of Pediatric Surgery Case Reports 2015 4 Pages PDF
Abstract

•Currarino syndrome (CS) is hereditary with autosomal dominant inheritance.•We present a rare pediatric case of CS associated with Hirschsprung's disease (HD).•The patient's mother had also been diagnosed as having incomplete CS.

We present a rare family consisting of a 10-month-old boy with complete Currarino syndrome associated with Hirschsprung's disease. His mother had been diagnosed as having incomplete Currarino syndrome. Only 11 cases of Currarino syndrome associated with Hirschsprung's disease have been reported in the literature. Our report suggests that it is necessary to perform preoperative examinations to rule out Hirschsprung's disease, if the patient presents with a history of severe defecation disorders from early childhood.

Related Topics
Health Sciences Medicine and Dentistry Perinatology, Pediatrics and Child Health
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