Malformations of Cortical Development: Difference between revisions
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* group II: abnormal neuronal migration | * group II: abnormal neuronal migration | ||
* group III: abnormal cortical organization | * group III: abnormal cortical organization | ||
{| class="wikitable" | |||
|- | |||
! Group !! Characteristics !! Conditions | |||
|- | |||
| Group I || abnormal proliferation of neuronal and glial cells || | |||
* Microcephaly | |||
* macrocephaly | |||
* FCDs without and with balloon cells (Taylor dysplasia types IIa and IIb), | |||
* hemimegalencephaly, | |||
* tuberous sclerosis, | |||
* dysembryoplastic neuroepithelial tumors (DNETs), gangliogliomas, gangliocytomas | |||
|- | |||
| Group II || abnormal neuronal migration || | |||
* Lissencephaly | |||
* heterotopias | |||
|- | |||
| Group III || abnormal cortical organization || | |||
* Polymicrogyria, | |||
* schizencephaly, | |||
* type I FCDs, | |||
* mild MCDs | |||
|} |
Revision as of 09:33, 22 May 2024
Categories
- group I: abnormal cell proliferation or apoptosis
- group II: abnormal neuronal migration
- group III: abnormal cortical organization
Group | Characteristics | Conditions |
---|---|---|
Group I | abnormal proliferation of neuronal and glial cells |
|
Group II | abnormal neuronal migration |
|
Group III | abnormal cortical organization |
|