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Congenital Disorder

Malformations of Cortical Development, Group I

AMW:DIS:100389

Cortical malformations secondary to abnormal neuronal and glial CELL PROLIFERATION or APOPTOSIS in NEUROGENESIS. This group includes congenital MICROCEPHALIES; MICROLISSENCEPHALIES, megalencephalies, HEMIMEGALENCEPHALIES and cortical dysplasias with balloon cells.

Pathology clinical
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Malformations of Cortical Development, Group I has parent Malformations of Cortical Development
Tuberous Sclerosis has parent Malformations of Cortical Development, Group I
Megalencephaly has parent Malformations of Cortical Development, Group I
Microcephaly has parent Malformations of Cortical Development, Group I
Focal Cortical Dysplasia has parent Malformations of Cortical Development, Group I
Hippocampal Sclerosis has parent Malformations of Cortical Development, Group I

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