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Two Cases of Right Congenital Diaphragmatic Anomaly.

Journal of the Korean Pediatric Society 1979;22(7):550-555.
Published online July 15, 1979.
Two Cases of Right Congenital Diaphragmatic Anomaly.
Hyun Kyung Cho1, Joon Sung Lee1, Jung Il Kim1, Mahn Kyoo Yang1, Ku Kim2, Seung Nam Kim2, Jae Sung Kim2
1Department of Pediatrics, Catholic Medical College, Seoul, Korea.
2Department of General Surgery, Catholic Medical College, Seoul, Korea.
우측 선천성 횡격막 기형 2 례
조현경1, 이준성1, 김정일1, 양만규1, 김동구2, 김승남2, 김재성2
1가톨릭의대 소아과학교실
2가톨릭의대’ 외과학교실
Congenital diaphragmatic anomaly is a rare congenital malformation and is found more frequently on the left side than right side. We had experienced two cases of comgenital diaphragmatic anomaly on the right side. One case was 8 months old male with congenital Bochdalek hernia and the other case was 17 months old female with congenital eventration of the diaphagm. The diagnosis was established by physical examination, chest X-ray, upper G-I series and other special studies. A brief review of the related literature was also presented.

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