Klinefelter syndrome (Q46922): Difference between revisions
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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 |
|---|---|---|---|
| default for all languages | 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. |
Statements
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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