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
  • 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