KMID : 0378019830260090050
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New Medical Journal 1983 Volume.26 No. 9 p.50 ~ p.54
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A Case of Apert¢¥s Syndrome (Acrocephalosyndactyly)
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Abstract
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Apert¢¥s syndrome is a rare disorder characterized by malformation of the skull (usually oxycephaly or acrocephaly), in association with systemic syndactyly.
It is due to congenital disturbance in the growth of bone and soft tissue affecting principally the head, the hand and the feet. This syndrome was first descirbed by Apert in 1906 since that time, over 200 cases have been reported.
The authors experienced one case of typical Apert¢¥s syndrome, and reviewed literatures briefly.
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