KMID : 0387519920020010221
|
|
Journal of Maryknoll Hospital 1992 Volume.2 No. 1 p.221 ~ p.228
|
|
A Case of Type II Lissencephaly ; Walker-Warburg Syndrome
|
|
±è¾Ö¿µ
ÀÌÁ¤È£/±è¿ë¼·/Á¶°æ¼÷/Á¶Á¾´ë
|
|
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
|
|
|
|
FullTexts / Linksout information
|
|
|
|
Listed journal information
|
|
|