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xyy

/ˌeks waɪ ˈwaɪ/

Traduction: Syndrome génétique masculin caractérisé par la présence d'un chromosome Y supplémentaire, aboutissant au caryotype 47,XYY.

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noun

/ˌeks waɪ ˈwaɪ/C1formalmedicalabréviation
  • frSyndrome génétique masculin caractérisé par la présence d'un chromosome Y supplémentaire, aboutissant au caryotype 47,XYY.

A medical and genetic term referring to a male chromosomal condition characterized by the presence of an extra Y chromosome, resulting in a 47,XYY karyotype.

indénombrable · nom propre

  1. Genetic conditionC1formalmedical

    A chromosomal condition in which a male has an extra Y chromosome, resulting in the 47,XYY karyotype.

    frSyndrome XYY (ou syndrome 47,XYY)

    • The XYY syndrome is often associated with above-average height.
    • Individuals with XYY may have normal development and no visible symptoms.
    • Genetic testing confirmed the presence of the XYY karyotype.