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KMID : 0391519930010020144
Journal of the Korean Child Neurology Society
1993 Volume.1 No. 2 p.144 ~ p.151
A Case of Menkes' syndrome




Abstract
Menkes' syndrome is a neurodegenerative disease of copper metabolism, which is inherited by X-linked pattern. The clinical manifestations and laboratory deficits are mostly explicable in term of failure of the numerous copper-dependent enzyme
systems.
The incidence is presumably in the range 1 in 50,000 to 1 in 1,000,000. Survival varies between 3 months-and 3-years, but is most often about 12 months.
We experienced one case of Menkes' syndrome in 2 months old male who had frequent seizure, abnormal hair, hypopigmentation and low serum copper level.
A review of literatures was also presented briefly.
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