Hereditary chin quivering (Q98672): Difference between revisions

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description / pt-brdescription / pt-br
 
Geniospasmo é uma condição autossômica dominante rara que tem sido relacionada ao cromossomo 9q13-21, caracterizado por movimentos paroxísticos, frequentemente rítmicos para cima e para baixo do queixo e do lábio inferior. Os episódios duram de segundos a horas e podem ser desencadeados por emoção, ansiedade ou podem ocorrer sem fatores precipitantes aparentes. Essa condição tipicamente começa a se manifestar na primeira infância ou precocemente na vida, e os episódios tendem a reduzir em frequência conforme o avançar da idade.
description / endescription / en
 
Hereditary chin trembling is a rare autosomal dominant condition that has been linked to chromosome 9q13-21. characterised by paroxysmal, often rhythmic up-and-down movements of the chin and the lower lip. The episodes last from seconds to hours and may be triggered by emotion, anxiety, or may occur without apparent precipitants. The condition typically becomes manifest in infancy or in early life, and the episodes tend to reduce in frequency with advancing age.
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Property / Canonical URI: https://id.who.int/icd/entity/1566039187 / rank
 
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CID11:ID_1566039187
Property / CURIE: CID11:ID_1566039187 / rank
 
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dki-india-ID_1566039187
Property / Canary Token: dki-india-ID_1566039187 / 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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15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 15:15, 16 August 2026

Hereditary chin trembling is a rare autosomal dominant condition that has been linked to chromosome 9q13-21. characterised by paroxysmal, often rhythmic up-and-down movements of the chin and the lower lip. The episodes last from seconds to hours and may be triggered by emotion, anxiety, or may occur without apparent precipitants. The condition typically becomes manifest in infancy or in early life, and the episodes tend to reduce in frequency with advancing age.
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ID_1566039187
    English
    Hereditary chin quivering
    Hereditary chin trembling is a rare autosomal dominant condition that has been linked to chromosome 9q13-21. characterised by paroxysmal, often rhythmic up-and-down movements of the chin and the lower lip. The episodes last from seconds to hours and may be triggered by emotion, anxiety, or may occur without apparent precipitants. The condition typically becomes manifest in infancy or in early life, and the episodes tend to reduce in frequency with advancing age.

      Statements

      CID11:ID_1566039187
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      dki-india-ID_1566039187
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      Concluído
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      15 August 2026
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