Isolated lissencephaly type 1 without known genetic defects (Q94690): Difference between revisions

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Lissencefalia tipo 1 isolada sem defeitos genéticos conhecidos pertence ao grupo geneticamente heterogêneo das lissencefalias clássicas. É um diagnóstico de exclusão, quando nem malformações associadas, nem histórico familiar são recuperados, na ausência de mutações em genes sabidamente envolvidos na lissencefalia clássica.
description / endescription / en
 
Isolated lissencephaly type 1 without known genetic defects belongs to the genetically heterogeneous group of classic lissencephalies. It is a diagnosis of exclusion, when neither associated malformations, nor family history is retrieved, in the absence of mutations of genes known to be involved in classic lissencephaly.
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Property / Canonical URI: https://id.who.int/icd/entity/80358651 / rank
 
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Property / CURIE
 
CID11:ID_80358651
Property / CURIE: CID11:ID_80358651 / rank
 
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Property / Canary Token
 
dki-india-ID_80358651
Property / Canary Token: dki-india-ID_80358651 / rank
 
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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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 10:04, 16 August 2026

Isolated lissencephaly type 1 without known genetic defects belongs to the genetically heterogeneous group of classic lissencephalies. It is a diagnosis of exclusion, when neither associated malformations, nor family history is retrieved, in the absence of mutations of genes known to be involved in classic lissencephaly.
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ID_80358651
    English
    Isolated lissencephaly type 1 without known genetic defects
    Isolated lissencephaly type 1 without known genetic defects belongs to the genetically heterogeneous group of classic lissencephalies. It is a diagnosis of exclusion, when neither associated malformations, nor family history is retrieved, in the absence of mutations of genes known to be involved in classic lissencephaly.

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      CID11:ID_80358651
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      dki-india-ID_80358651
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      Concluído
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      15 August 2026
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