Schizencephaly (Q46049): Difference between revisions
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| description / pt-br | description / pt-br | ||
Esquizencefalia é uma malformação cerebral congênita rara caracterizada pela presença de fendas lineares em um ou ambos os hemisférios do cérebro, estendendo-se dos ventrículos laterais à superfície pial do córtex, e que leva a uma variedade de sintomas neurológicos, como epilepsia, déficits motores e atraso psicomotor. | |||
| description / en | description / en | ||
Schizencephaly is a rare congenital cerebral malformation characterised by the presence of linear clefts in one or both hemispheres of the brain, extending from the lateral ventricles to the pial surface of the cortex, and that lead to a variety of neurological symptoms such as epilepsy, motor deficits, and psychomotor retardation. | |||
Revision as of 14:22, 13 August 2026
Schizencephaly is a rare congenital cerebral malformation characterised by the presence of linear clefts in one or both hemispheres of the brain, extending from the lateral ventricles to the pial surface of the cortex, and that lead to a variety of neurological symptoms such as epilepsy, motor deficits, and psychomotor retardation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA05.61 |
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| English | Schizencephaly |
Schizencephaly is a rare congenital cerebral malformation characterised by the presence of linear clefts in one or both hemispheres of the brain, extending from the lateral ventricles to the pial surface of the cortex, and that lead to a variety of neurological symptoms such as epilepsy, motor deficits, and psychomotor retardation. |
