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KMID : 0387519920020010221
Journal of Maryknoll Hospital
1992 Volume.2 No. 1 p.221 ~ p.228
A Case of Type II Lissencephaly ; Walker-Warburg Syndrome
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Abstract
Lissencephaly is a rare abnormality of brain development characterized by incomplete neuronal migration and a smooth cerebral surface. Three types of lissencephaly are reconized. Type I is characterized by microcephaly and dysmorphic facies. Type
II
usually lacks characteristic facies but exhibits macrocephaly from hydrocephalus, eye anomaly, and/or congenital muscular dystrophies. Type III is charactererized by microcephaly without any characteristic dysmorphic facial features.
We have experienced a case of type II lissencephaly(Walker-Warbur syndrome). In this case of lissencephaly hydrocephalus, hypoplasia of corpus callosum, hypoplasia of septum pellucidum, retinal dysplasia, potic atrophy and nystagmus was noticed.
So
we
present this case with a review of referential literatures.
KEYWORD
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