Malformations of Cortical Development: Difference between revisions

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(Created page with "Categorized into three groups: {| class="wikitable" |- ! Group !! Characteristics !! Conditions |- | Group I || Malformations resulting from 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 || Malformations resulting from abnormal neu...")
 
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Categorized into three groups:
= Categories =
{| class="wikitable"
{| class="wikitable"
|-
|-
! Group !! Characteristics !! Conditions
! Group !! Characteristics !! Conditions
|-
|-
| Group I || Malformations resulting from 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 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 || Malformations resulting from abnormal neuronal migration || Lissencephaly, heterotopias
| Group II || abnormal neuronal migration ||
* Lissencephaly
* heterotopias
|-
|-
| Group III || Malformations resulting from abnormal cortical organization || Polymicrogyria, schizencephaly, type I FCDs, mild MCDs
| Group III || abnormal cortical organization ||
* Polymicrogyria,  
* schizencephaly,  
* type I FCDs,  
* mild MCDs
|}
|}

Revision as of 09:27, 22 May 2024

Categories

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
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