Familial infantile bilateral striatal necrosis (Q107470): Difference between revisions

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A necrose estriatal bilateral infantil familiar é a forma familiar de necrose estriado bilateral infantil (NEBI), uma síndrome de degeneração esponjosa simétrica bilateral do núcleo caudado, putâmen e globo pálido e é caracterizada por regressão do desenvolvimento, coreoatetose e distonia que progride para quadriparesia espástica.
description / endescription / en
 
Familial infantile bilateral striatal necrosis is the familial form of infantile bilateral striatal necrosis (IBSN), a syndrome of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus and is characterised by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis.
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Property / Canonical URI: https://id.who.int/icd/entity/1873983370 / rank
 
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CID11:ID_1873983370
Property / CURIE: CID11:ID_1873983370 / rank
 
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dki-india-ID_1873983370
Property / Canary Token: dki-india-ID_1873983370 / rank
 
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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16 August 2026
Timestamp+2026-08-16T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 14:27, 17 August 2026

Familial infantile bilateral striatal necrosis is the familial form of infantile bilateral striatal necrosis (IBSN), a syndrome of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus and is characterised by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis.
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ID_1873983370
    English
    Familial infantile bilateral striatal necrosis
    Familial infantile bilateral striatal necrosis is the familial form of infantile bilateral striatal necrosis (IBSN), a syndrome of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus and is characterised by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis.

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      CID11:ID_1873983370
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      dki-india-ID_1873983370
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      Concluído
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      16 August 2026
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