"Porencephaly" 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 characterized by white matter-lined cleft or cyst associated with ISCHEMIA and hemorrhagic insults. Symptoms include delayed growth and development, HYPOTONIA; SEIZURES; SPASTIC HEMIPLEGIA and MACROCEPHALY; MICROCEPHALY; or HYDROCEPHALUS. Mutations in the genes encoding COLLAGEN TYPE IV are associated with familial types.
- Encephaloclastic Porencephaly
- Porencephaly, Encephaloclastic
- Porencephaly, Familial
- Porencephaly, Type 1, Autosomal Dominant
- Familial Porencephalic White Matter Disease
- Infantile Hemiplegia with Porencephaly
- Porencephaly Type 1
- Porencephaly Type 1s
- Familial Porencephaly
- Porencephaly, Type 1
- Type 1 Porencephaly
- Autosomal Dominant Porencephaly Type 1
Below are MeSH descriptors whose meaning is more general than "Porencephaly".
Below are MeSH descriptors whose meaning is more specific than "Porencephaly".
This graph shows the total number of publications written about "Porencephaly" by people in this website by year, and whether "Porencephaly" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.