Pierre Robin syndrome (Q46699): Difference between revisions
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A síndrome de Pierre-Robin (ou sequência de Pierre-Robin) é caracterizada por tríade de anomalias morfológicas orofaciais que consiste em retrognatismo, glossoptose e fenda velopalatal mediana posterior. Essa condição é chamada de sequência porque a fenda palatina posterior é um defeito secundário associado a desenvolvimento mandibular anormal: a hipoplasia mandibular ocorrendo no início da gestação faz com que a língua seja mantida elevada na cavidade oral, impedindo a fusão das prateleiras palatinas. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. This condition is referred to as a sequence because the posterior cleft palate is a secondary defect associated with abnormal mandibular development: mandibular hypoplasia occurring early in gestation causes the tongue to be maintained high-up in the oral cavity, preventing fusion of the palatal shelves. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/136361299 / rank | |||||||||||||||
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CID11:LA56 | |||||||||||||||
| Property / CURIE: CID11:LA56 / rank | |||||||||||||||
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dki-india-LA56 | |||||||||||||||
| Property / Canary Token: dki-india-LA56 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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| Property / Linked ICD 10: EDUARDO JORGE CURY / rank | |||||||||||||||
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Latest revision as of 15:28, 13 August 2026
Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. This condition is referred to as a sequence because the posterior cleft palate is a secondary defect associated with abnormal mandibular development: mandibular hypoplasia occurring early in gestation causes the tongue to be maintained high-up in the oral cavity, preventing fusion of the palatal shelves.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA56 |
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| English | Pierre Robin syndrome |
Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. This condition is referred to as a sequence because the posterior cleft palate is a secondary defect associated with abnormal mandibular development: mandibular hypoplasia occurring early in gestation causes the tongue to be maintained high-up in the oral cavity, preventing fusion of the palatal shelves. |
Statements
CID11:LA56
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dki-india-LA56
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Concluído
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13 August 2026
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