No abstract available.
Malformations of Cortical Development*

No abstract available.
Classification* ; Malformations of Cortical Development*

No abstract available.
Malformations of Cortical Development* ; Seizures*

No abstract available.
Malformations of Cortical Development* ; Seizures*

No abstract available.
Animals ; Malformations of Cortical Development* ; Rats*

PURPOSE: The study was to evaluate the localization of the abnormal gyral and sulcal patterns obtained by means of brain surface rendering imaging. MATERIALS AND METHODS: Nineteen patients with cortical dysplasia who underwent brain surface rendering MR imaging were included in this study. We acquired MP-RAGE sequence and created the 3-D surface rendering MR images by using VoxelPlus(R). Anatomical locations and configurations of abnormal gyri and sulci were reviewed. RESULTS: Abnormal gyral and sulcal patterns were seen 18 in 19 patients. The configuration and orientation of affected gyri and sulci were clearly evaluated in the brain surface rendering images. In a lissencephaly, the a cortex was not delineated and showed markedly thick and smooth gyral pattern. In a schizencephaly, there were wheel shaped broad gyral pattern around the cleft. In a hemimegalencephaly, an affected hemisphere were enlarged and displayed thick and wide gyral pattern. In CBPS, the insular cortex was exposed and the gyri of the lesion were thickened. In focal cortical dysplasia, there were irregular serrated or thick and enlarged gyri. CONCLUSION: Brain surface rendering MR imaging is useful for the evaluation of a detailed gyral pattern and accurate involvement site of abnormal gyri.
Brain ; Humans ; Lissencephaly ; Malformations of Cortical Development ; Orientation

No abstract available.
Magnetic Resonance Imaging ; Malformations of Cortical Development*

The advent of MRI enables us to make an in-vivo diagnosis of cortical dysplastic lesions which are highly epileptogenic and show the variety of seizure patterns. Authors report a case of rolandic cortical dysplasia who had highly intractable focal motor clonic seizures. Invasive recording with subdural grid was very helpful in delinating the epileptogenic area as well as in function mapping of eloquent areas. Total removal of dysplastic lesion could treat this highly intractable epilepsy succesfully.
Diagnosis ; Epilepsy ; Magnetic Resonance Imaging ; Malformations of Cortical Development* ; Seizures

Microgyria is one type of cortical dysplasia with dyslaminations and anomalous cell densities, which could be produced experimentally. In a normal rat cortical development, overproduced neuroblasts gradually die by apoptosis. Thus, the diminished apoptosis may lead to the anomalous cell densities and dyslaminations. This study examined the ontogeny of cell densities in rat microgyria, in homotopic contralateral cortex and in control cortex. Multiple applications of cold probe (-70degrees C) on the right hemisphere in postnatal day (PN) 0 rat pups produced unilateral microgyria. Cell densities had decreased from PN 1 to 2 in microgyria, in the contralateral left hemisphere, and in the control cortex. From PN3 to PN10, while the cell density of the microgyria had increased (p<0.001), cell densities of the control and homotopic area continued to decrease. Apoptosis was greater in the microgyria than in the control and left hemisphere from PN1 to 3 and then remarkably decreased (p<0.001). These results suggest that the increased cell density in microgyria is not from decreased apoptosis, but probably caused by the increased proliferation or migration.
Animals ; Apoptosis* ; Cell Count ; Cell Movement ; Malformations of Cortical Development* ; Rats*

Yakovlev demonstrated that the Schizencephalies appear to result from injury to developing cerebral vesicles in the second month of intrauterine life. There is a total loss of neurons in restricted symmetrical zones of each developing hemisphere and on either side of the resulting cleft-shaped defects are evidences of subtotal injury to developing neuroblasts. A case of a 4 years old male with Schizencephaly is reported.
Child, Preschool ; Humans ; Male ; Malformations of Cortical Development* ; Neurons