"Hemimegalencephaly" 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.
Rare MALFORMATIONS OF CORTICAL DEVELOPMENT, GROUP I characterized by the enlargement of one side of the brain. It is associated with seizures, partial paralysis, and mental retardation.
Descriptor ID |
D065705
|
MeSH Number(s) |
C05.660.207.536.500 C10.500.507.400.249.500 C16.131.621.207.532.500 C16.131.666.507.400.249.500
|
Concept/Terms |
Hemimegalencephaly- Hemimegalencephaly
- Hemimegalencephalies
- Unilateral Macrocephaly
- Macrocephalies, Unilateral
- Macrocephaly, Unilateral
- Unilateral Macrocephalies
- Unilateral Megalencephaly
- Megalencephalies, Unilateral
- Megalencephaly, Unilateral
- Unilateral Megalencephalies
|
Below are MeSH descriptors whose meaning is more general than "Hemimegalencephaly".
Below are MeSH descriptors whose meaning is more specific than "Hemimegalencephaly".
This graph shows the total number of publications written about "Hemimegalencephaly" by people in this website by year, and whether "Hemimegalencephaly" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemimegalencephaly" by people in Profiles.
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Clinical pitfalls in the diagnosis of segmental overgrowth syndromes: a child with the c.2740G > A mutation in PIK3CA gene. Ital J Pediatr. 2018 Sep 19; 44(1):110.