Chromosomes fail to separate
properly, causing a nondisjunction.
This results in cells having an extra
copy of a chromosome, specifically
Chromosome 21. It is the MOST
COMMON cause for Down
Syndrome.
Translocation
Anotações:
A whole Chromosome 21 is
attached to another
chromosome (i.e. an extra
copy is attached elsewhere),
which results in a structural
abnormality causing Down
Syndrome. It is much rarer
than Trisomy 21.
Mosaicism
Anotações:
After the fertilization of egg and sperm cells, one
line of cells replicate properly. However, the other line
of cells doesn't, and they have an extra copy of
Chromosome 21. This results in Down Syndrome, but
the effects are less severe than the other causes as
the DNA is incorrect in only some cells. This is the
RAREST method of inheriting Down Syndrome.