45, X, 46, XY gonadal dysgenesis (Q84783): Difference between revisions

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Disgenesia gonadal mista 45,X/46,XY é um distúrbio do desenvolvimento sexual (DDS) associado a uma anormalidade numérica do cromossomo sexual resultante de mosaicismo do cromossomo Y e levando a desenvolvimento gonadal anormal. A prevalência é desconhecida. As manifestações clínicas são altamente variáveis, desde virilização parcial e genitália ambígua ao nascimento até pacientes com fenótipo completamente masculino ou feminino.
description / endescription / en
 
45,X/46,XY mixed gonadal dysgenesis is a disorder of sex development (DSD) associated with a numerical sex chromosome abnormality resulting from Y-chromosome mosaicism and leading to abnormal gonadal development. Prevalence is unknown. The clinical manifestations are highly variable, ranging from partial virilization and ambiguous genitalia at birth to patients with a completely male or female phenotype.
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Property / Canonical URI: https://id.who.int/icd/entity/451241641 / rank
 
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CID11:ID_451241641
Property / CURIE: CID11:ID_451241641 / rank
 
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dki-india-ID_451241641
Property / Canary Token: dki-india-ID_451241641 / 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
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 10:08, 15 August 2026

45,X/46,XY mixed gonadal dysgenesis is a disorder of sex development (DSD) associated with a numerical sex chromosome abnormality resulting from Y-chromosome mosaicism and leading to abnormal gonadal development. Prevalence is unknown. The clinical manifestations are highly variable, ranging from partial virilization and ambiguous genitalia at birth to patients with a completely male or female phenotype.
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ID_451241641
    English
    45, X, 46, XY gonadal dysgenesis
    45,X/46,XY mixed gonadal dysgenesis is a disorder of sex development (DSD) associated with a numerical sex chromosome abnormality resulting from Y-chromosome mosaicism and leading to abnormal gonadal development. Prevalence is unknown. The clinical manifestations are highly variable, ranging from partial virilization and ambiguous genitalia at birth to patients with a completely male or female phenotype.

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      CID11:ID_451241641
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      dki-india-ID_451241641
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      Concluído
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      13 August 2026
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