xyy

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xyy

A male with an XYY karyotype undergoes a routine genetic screening.

Definition
  1. Noun:
    • (Genetics): An abnormal chromosomal complement in a male, characterized by the presence of an extra Y chromosome, resulting in a 47,XYY karyotype.
Usage
  • The term "xyy" is used specifically in the fields of genetics, medicine, and biology to describe a chromosomal condition.
  • It functions as a noun, often preceded by articles like "an" or "the," or used attributively (e.g., XYY syndrome).
  • Example:
Examples
  • As a subject:
    • Xyy is a chromosomal anomaly that occurs in a small percentage of the male population.
  • As an object:
    • The test confirmed the presence of xyy in the fetus's cells.
  • Attributive use:
    • Researchers are studying the developmental outcomes of xyy individuals.
Advanced Usage
  • "XYY syndrome": The clinical condition associated with the 47,XYY karyotype.
    • The pediatrician discussed the potential characteristics of XYY syndrome with the parents.
  • "47,XYY": The formal scientific notation for the karyotype.
    • The lab report listed the chromosomal finding as 47,XYY.
Variants and Related Words
  • 47,XYY karyotype (n): The formal genetic description.
  • XYY syndrome (n): The medical condition associated with the chromosomal complement.
Synonyms
  • 47,XYY: (The precise scientific synonym)
  • Double Y syndrome: (An informal, less common term)
Notes on Meaning
  • The term "xyy" refers strictly to a genetic constitution. It is not a term for a disease or illness, but rather a description of a chromosomal variation.
  • It is distinct from other sex chromosome aneuploidies like XXY (Klinefelter syndrome) or XXX.
xyy

A male with an XYY karyotype undergoes a routine genetic screening.

Noun
  1. (genetics) abnormal complement of sex hormones in a male who has two Y chromosomes

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