 Polymicrogyria
"Polymicrogyria" 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.
Heterogeneous disorders of cortical malformation characterized by excessive and small fused gyri and shallow sulci of the CORTEX with abnormal cortical lamination. It is considered a malformation secondary to abnormal post-migrational development of the neurons during cerebral cortical development and is associated with EPILEPSY and learning difficulties.
| Descriptor ID |
D065706
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| MeSH Number(s) |
C10.500.507.500.500 C16.131.666.507.500.500
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| Concept/Terms |
Polymicrogyria- Polymicrogyria
- Polymicrogyrias
- Micropolygyria
- Micropolygyrias
- Cerebral Micropolygyria
- Cerebral Micropolygyrias
- Micropolygyria, Cerebral
- Micropolygyrias, Cerebral
- Cerebral Polymicrogyria
- Cerebral Polymicrogyrias
- Polymicrogyria, Cerebral
- Polymicrogyrias, Cerebral
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Below are MeSH descriptors whose meaning is more general than "Polymicrogyria".
Below are MeSH descriptors whose meaning is more specific than "Polymicrogyria".
This graph shows the total number of publications written about "Polymicrogyria" by people in this website by year, and whether "Polymicrogyria" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2019 | 0 | 1 | 1 | | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Polymicrogyria" by people in Profiles.
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Shelkowitz E, Stence NV, Neuberger I, Park KL, Saenz MS, Pao E, Oyama N, Friedman SD, Shaw DWW, Mirzaa GM. Variants in PTEN Are Associated With a Diverse Spectrum of Cortical Dysplasia. Pediatr Neurol. 2023 10; 147:154-162.
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Davis S, Ware MA, Zeiger J, Deardorff MA, Grand K, Grimberg A, Hsu S, Kelsey M, Majidi S, Matthew RP, Napier M, Nokoff N, Prasad C, Riggs AC, McKinnon ML, Mirzaa G. Growth hormone deficiency in megalencephaly-capillary malformation syndrome: An association with activating mutations in PIK3CA. Am J Med Genet A. 2020 01; 182(1):162-168.
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