Klinefelter syndrome (Q46922): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1937385304 / rank
 
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CID11:LD50.3
Property / CURIE: CID11:LD50.3 / rank
 
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dki-india-LD50.3
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Concluído
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10: DIEGO GAMARRA MOREIRA / rank
 
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Latest revision as of 15:49, 13 August 2026

Klinefelter syndrome defines a group of chromosomal disorders in which there is at least one extra X chromosome compared with the normal 46,XY male karyotype. The effects on physical features and on physical and cognitive development increase with the number of extra X's, and each extra X is associated with an intelligence quotient (IQ) decrease of approximately 15-16 points, with language most affected, particularly expressive language skills.
Language Label Description Also known as
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LD50.3
    English
    Klinefelter syndrome
    Klinefelter syndrome defines a group of chromosomal disorders in which there is at least one extra X chromosome compared with the normal 46,XY male karyotype. The effects on physical features and on physical and cognitive development increase with the number of extra X's, and each extra X is associated with an intelligence quotient (IQ) decrease of approximately 15-16 points, with language most affected, particularly expressive language skills.

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      CID11:LD50.3
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      dki-india-LD50.3
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      Concluído
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      13 August 2026
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