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A Case of Edward Syndrom.

Journal of the Korean Pediatric Society 1989;32(3):396-401.
Published online March 31, 1989.
A Case of Edward Syndrom.
Youn Hong Choi, Hyun Joo Choi, Eun Hwa Shin, Ju Hong Cha, Kwang Jeon Kim
Department of Pediatrics, Chung Gu Sung Sim Hospital, Seoul, Korea
Edward Syndrome 1례
최연홍, 최현주, 신은화, 차주홍, 김광전
청구성심병원 소아과
Received: 20 August 1988   • Accepted: 6 September 1988
Edward syndrome is known as 18-trisomy with multiple congenital anomalies. Recently, we experienced a case of 18-trisomy syndrome in a new-born female baby who was born at Chung Gu Sung Sim Hospital. Grossly this baby had multiple anomalies which were characterized by prominent occiput, hypertelorism, small palpebral fissure, small oral opening, high arched palate, micrognathia, low-set malformed ear, rocker bottom feet, narrow pelvis, limited hip abduction, dark colored prominent labia minora and single umbilical artery. Karyotyping and Chromosomal analysis revealed 47, XX, + 18. On autopsy, horseshoe kidney was found. A brief review of literature was presented.
Key Words: Edward Syndrome

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