X as in X
chromosome
The X chromosome
is one of the two sex-determining chromosomes in many animal species, including
mammals (the other is the Y chromosome).
T he X
chromosome was named for its unique properties by early researchers,
which resulted in the naming of its counterpart Y chromosome, for the next letter in the alphabet, after it was
discovered later.
Each person
normally has one pair of sex chromosomes in each cell. Females have two X chromosomes, whereas males have
one X
and one Y chromosome. Both males and
females retain one of their mother's X chromosomes, and females retain their second X chromosome
from their father. Since the father
retains his X
chromosome from his mother, a human female has one X chromosome from her paternal
grandmother (father's side), and one X chromosome from her mother.
The typical
number of chromosomes in a human cell is 46 -- two pairs of 23 -- holding an
estimated 25,000 genes. One set of 23 chromosomes is inherited from the
biological mother (from the egg), and the other set is inherited from the
biological father (from the sperm).
A chromosome abnormality reflects an abnormality of chromosome number
or structure, i.e. when an individual is missing either a chromosome from a
pair (monosomy) or has more than two chromosomes of a pair (trisomy).
An example of a condition
caused by numerical abnormalities is Down Syndrome, also known as Trisomy 21
(an individual with Down Syndrome has three copies of chromosome 21, rather
than two). Turner Syndrome is an example
of monosomy, where the individual - in this case a female - is born with only
one sex chromosome, an X.
Isn’t it unbelievable how our bodies function? Be aware every day of this wonder, keep your
body healthty and treat it with respect.
You only have one!
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