Carey-Fineman-Ziter syndrome (Q94118): Difference between revisions

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A síndrome de Carey-Fineman-Ziter é uma condição rara caracterizada pela associação de hipotonia, sequência de Moebius (paralisia facial congênita bilateral com comprometimento da abdução ocular), sequência de Pierre-Robin (micrognatia, glossoptose e palato ogival ou fenda palatina), face incomum e retardo de crescimento.
description / endescription / en
 
Carey-Fineman-Ziter syndrome is a rare condition characterised by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1784462638 / rank
 
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Property / CURIE
 
CID11:ID_1784462638
Property / CURIE: CID11:ID_1784462638 / rank
 
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Property / Canary Token
 
dki-india-ID_1784462638
Property / Canary Token: dki-india-ID_1784462638 / 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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 09:14, 16 August 2026

Carey-Fineman-Ziter syndrome is a rare condition characterised by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay.
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ID_1784462638
    English
    Carey-Fineman-Ziter syndrome
    Carey-Fineman-Ziter syndrome is a rare condition characterised by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay.

      Statements

      CID11:ID_1784462638
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      dki-india-ID_1784462638
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      Concluído
      0 references
      15 August 2026
      0 references