"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
|
| MeSH Number(s) |
C10.500.507.500.500 C16.131.666.507.500.500
|
| Concept/Terms |
Polymicrogyria- Polymicrogyria
- Polymicrogyrias
- Micropolygyria
- Micropolygyrias
- Cerebral Micropolygyria
- Cerebral Micropolygyrias
- Micropolygyria, Cerebral
- Micropolygyrias, Cerebral
- Cerebral Polymicrogyria
- Cerebral Polymicrogyrias
- Polymicrogyria, Cerebral
- Polymicrogyrias, Cerebral
|
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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 2 | 1 | 3 |
| 2021 | 3 | 0 | 3 |
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Below are the most recent publications written about "Polymicrogyria" by people in Profiles.
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The Names of Things: The 2018 Bernard Sachs Lecture. Pediatr Neurol. 2021 09; 122:41-49.
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ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria. Brain. 2021 06 22; 144(5):1435-1450.
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Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes. Am J Med Genet A. 2021 09; 185(9):2719-2738.
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Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome? Am J Med Genet A. 2020 10; 182(10):2207-2213.
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Defining the phenotypical spectrum associated with variants in TUBB2A. J Med Genet. 2021 01; 58(1):33-40.
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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
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Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics. Brain. 2019 04 01; 142(4):867-884.
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De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain. 2018 03 01; 141(3):698-712.
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Ultra-high-field MR imaging in polymicrogyria and epilepsy. AJNR Am J Neuroradiol. 2015 Feb; 36(2):309-16.