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A Case of Apert's Syndrome.

Journal of the Korean Pediatric Society 1986;29(9):1002-1006.
Published online September 30, 1986.
A Case of Apert's Syndrome.
In Kwyu Park, Kang Ho Kim, Yeong Bong Park, Jin Heon Kim, Chang Soo Ra
Department of Pediatrics, College of Medicine, Chosun University Kwang ]u,Korea
Apert 증후군 (Acrocephalosyndactyly) 1례
박인규, 김강호, 박영봉, 김진헌, 나창수
조선대학교 의과대학 소아과교실
Apert’s syndrome is an uncommon, congenital disturbance in the growth of bone and soft tissue affecting principally the head, the hand and feet. So there is skull malformation, most often acrocephaly, associated with symmetrical malformation of both hand and feet. This syndrome was first described by Apert in 1906. since that time, over 200 cases have been reported in the world. Recently, we have experienced a case of newborn infant, male, who was found to have congenital anomalies of the skull and extremites, characteristic of the Apert's syndromee. A brief review of literature was made.
Key Words: Apert’s syndrome, Acrocephaly, Syndactyly

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