Schizencephaly (Q46049): Difference between revisions

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description / pt-brdescription / 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 / endescription / 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.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1693546163 / rank
 
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Property / CURIE
 
CID11:LA05.61
Property / CURIE: CID11:LA05.61 / rank
 
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Property / Canary Token
 
dki-india-LA05.61
Property / Canary Token: dki-india-LA05.61 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: Q07.9 / rank
 
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Latest revision as of 14:23, 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
    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.

      Statements

      CID11:LA05.61
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      dki-india-LA05.61
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      Concluído
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      13 August 2026
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      0 references