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Porencephaly MeSH Descriptor Data 2023


MeSH Heading
Porencephaly
Tree Number(s)
C05.660.207.620.500
C10.500.507.500.625
C16.131.621.207.620.500
C16.131.666.507.500.625
Unique ID
D065708
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D065708
Scope Note
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.
Entry Term(s)
Autosomal Dominant Porencephaly Type 1
Brain Small Vessel Disease With Axenfeld-Rieger Anomaly
Brain Small Vessel Disease with Hemorrhage
Brain Small-Vessel Disease with Hemorrhage
Col4a1-Related Brain Small-Vessel Disease
Congenital Porencephaly
Developmental Porencephaly
Encephaloclastic Porencephaly
Familial Porencephalic White Matter Disease
Familial Porencephaly
Infantile Hemiplegia with Porencephaly
Leukoencephalopathy with Axenfeld-Rieger Anomaly
Porencephaly Type 1
Porencephaly, Familial
Porencephaly, Type 1
Porencephaly, Type 1, Autosomal Dominant
Post-traumatic Porencephaly
Posttraumatic Porencephaly
Retinal Arteriolar Tortuosity, Infantile Hemiparesis, and Leukoencephalopathy, Autosomal Dominant
Previous Indexing
Brain Diseases (1963-2014)
See Also
Collagen Type IV
Public MeSH Note
2015
History Note
2015
Date Established
2015/01/01
Date of Entry
2014/06/26
Revision Date
2021/05/10
Porencephaly Preferred
Porencephaly, Type 1 Narrower
Congenital Porencephaly Narrower
Developmental Porencephaly Narrower
Encephaloclastic Porencephaly Narrower
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