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KMID : 1152420210270010022
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Advances in Pediatric Surgery
2021 Volume.27 No. 1 p.22 ~ p.26
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Large Congenital Epigastric Hernia with DiGeorge Syndrome: A Case Report
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Kim Hee-Ju
Chung Jae-Hee
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Abstract
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Chromosome 22q11.2 deletion syndrome is common and presents with multiple congenital anomalies ranging from congenital heart disease to cognitive and neuropsychiatric conditions. Congenital large epigastric hernia is extremely rare in neonates. We present a case of a large congenital epigastric hernia in a neonate with DiGeorge syndrome.
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KEYWORD
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Abdominal hernia, 22q11.2 deletion syndrome, DiGeorge syndrome
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