Malformations of Cortical Development, Group II
"Malformations of Cortical Development, Group II" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICULAR NODULAR HETEROTOPIA.
| Descriptor ID |
D054081
|
| MeSH Number(s) |
C10.500.507.450 C16.131.666.507.450
|
| Concept/Terms |
Malformations of Cortical Development, Group II- Malformations of Cortical Development, Group II
- Malformations Secondary to Abnormal Neuronal Migration
- Malformations Due to Abnormal Neuronal Migration
- Cortical Malformations, Group II
- Neuronal Migration Disorders
- Disorder, Neuronal Migration
- Disorders, Neuronal Migration
- Migration Disorder, Neuronal
- Migration Disorders, Neuronal
- Neuronal Migration Disorder
|
Below are MeSH descriptors whose meaning is more general than "Malformations of Cortical Development, Group II".
Below are MeSH descriptors whose meaning is more specific than "Malformations of Cortical Development, Group II".
This graph shows the total number of publications written about "Malformations of Cortical Development, Group II" by people in this website by year, and whether "Malformations of Cortical Development, Group II" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 1 | 0 | 1 |
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Below are the most recent publications written about "Malformations of Cortical Development, Group II" by people in Profiles.
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Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. Brain. 2013 Nov; 136(Pt 11):3378-94.