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Apert씨 증후군 1예
A Case of Aperts Syndrome
유명숙(MS Yoo),차인환(IW Cha),박인서(IS Park)
UCI I410-ECN-0102-2009-510-005378066

본원 산부인과에서 전형적인 Apert씨 증후군 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

Aperts syndrome is an uncommon, congenital disturbance in the growth of bone and soft tisue affecting principally the head, the hands and the feet, therefore, there is skull malformation, most often oxycephaly, associated with malformation of both hands and feet. This syndrome was first described by Apert in 1906. From then on, over 200 cases have been reported. Recently we have experienced one case of typical Aperts syndrome.

[자료제공 : 네이버학술정보]
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