Ochoa syndrome (Q94188): Difference between revisions

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A síndrome de Ochoa é uma síndrome genética caracterizada pela associação de disfunção miccional grave e uma expressão facial característica. Pacientes com síndrome de Ochoa apresentam incontinência, infecção do trato urinário e hidronefrose. A disfunção miccional é o resultado de uma uropatia obstrutiva. O peculiar dismorfismo facial está relacionado a uma inversão incomum da expressão facial que ocorre quando a criança sorri ou chora.
description / endescription / en
 
Ochoa syndrome is a genetic syndrome characterised by the association of severe voiding dysfunction and a characteristic facial expression. Patients with Ochoa syndrome present with incontinence, urinary tract infection and hydronephrosis. Voiding dysfunction is the result of an obstructive uropathy. The peculiar facial dysmorphism is related to an unusual inversion of facial expression that occurs when the child smiles or cries.
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Property / Canonical URI: https://id.who.int/icd/entity/443886910 / rank
 
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CID11:ID_443886910
Property / CURIE: CID11:ID_443886910 / rank
 
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dki-india-ID_443886910
Property / Canary Token: dki-india-ID_443886910 / 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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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 09:18, 16 August 2026

Ochoa syndrome is a genetic syndrome characterised by the association of severe voiding dysfunction and a characteristic facial expression. Patients with Ochoa syndrome present with incontinence, urinary tract infection and hydronephrosis. Voiding dysfunction is the result of an obstructive uropathy. The peculiar facial dysmorphism is related to an unusual inversion of facial expression that occurs when the child smiles or cries.
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ID_443886910
    English
    Ochoa syndrome
    Ochoa syndrome is a genetic syndrome characterised by the association of severe voiding dysfunction and a characteristic facial expression. Patients with Ochoa syndrome present with incontinence, urinary tract infection and hydronephrosis. Voiding dysfunction is the result of an obstructive uropathy. The peculiar facial dysmorphism is related to an unusual inversion of facial expression that occurs when the child smiles or cries.

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      CID11:ID_443886910
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      dki-india-ID_443886910
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      Concluído
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      15 August 2026
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