Malformations of Cortical Development, Group I

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.

Year introduced: 2015

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C10.500.507.400, C16.131.666.507.400

MeSH Unique ID: D065703

Entry Terms:

• Abnormal Proliferation Cortical Malformations
• Cortical Malformations, Group I
• Malformations Secondary to Abnormal Neuronal and Glial Proliferation or Apoptosis
• Malformations Due to Abnormal Neuronal and Glial Proliferation or Apoptosis

Previous Indexing:

• Cerebral Cortex/abnormalities (1995-2007)
• Malformations of Cortical Development (2008-2014)

All MeSH Categories
Diseases Category
Nervous System Diseases
Nervous System Malformations
Malformations of Cortical Development
Malformations of Cortical Development, Group I
Focal Cortical Dysplasia
Hippocampal Sclerosis
Megalencephaly
Hemimegalencephaly
Microcephaly
Tuberous Sclerosis

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Malformations of Cortical Development
Malformations of Cortical Development, Group I
Focal Cortical Dysplasia
Hippocampal Sclerosis
Megalencephaly
Hemimegalencephaly
Microcephaly
Tuberous Sclerosis