"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
|
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 |
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2015 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Polymicrogyria" by people in Profiles.
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Maternal mosaicism underlies the inheritance of a rare germline AKT3 variant which is responsible for megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome in two Roma half-siblings. Exp Mol Pathol. 2020 08; 115:104471.
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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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De novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia. Eur J Hum Genet. 2016 08; 24(9):1359-62.
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Surgical management of medically refractory epilepsy in patients with polymicrogyria. Epilepsia. 2016 Jan; 57(1):151-61.
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Failure to Identify the Left Arcuate Fasciculus at Diffusion Tractography Is a Specific Marker of Language Dysfunction in Pediatric Patients with Polymicrogyria. Behav Neurol. 2015; 2015:351391.