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extracts
from an article by Kenneth H Neldner MD
It has been
known for well over 50 years that PXE is a hereditary disorder that
is passed from one generation to the next through the genes, although
the specific details are complex and not totally understood. It is
accepted, however, that the PXE gene passes only recessively; it is
never a dominant gene.
In Rececessive
(AR) inheritance, it takes two defective recessive genes - one from
each parent - to produce the disorder. The parents who are carriers
of the PXE gene, may be totally unaware of the fact that they are
carrying a PXE gene. The children of two parents who each carry
the PXE gene will have a 25% chance of getting a PXE gene from each
parent and will then develop PXE; 50% of the children will only
get one PXE gene and will be carriers but will not develop PXE;
25% will get two completely normal genes. Once again these are statistical
odds, based on large numbers, so any family with four children,
for example, would not necessarily have a genetic split as presented,
unless there were at least a hundred children! In AR inheritance,
it is also quite common to see two or more affected siblings in
a family, but again, their parents and the children of the affected
siblings should not have PXE. An illustration of the three examples
of recessive inheritance is shown below.

There are three
possible situations shown, using diamond-shaped outlines to indicate
either male or female. The X-shaped structures represent chromosomes.
The blackened chromosomes carry the PXE gene and a darkened diamond
means that the person has PXE. The upper left example "A" shows
how a recessive chromosome (carrying a PXE gene) can be transmitted
from generation to generation without anyone developing PXE. lf
only one parent has the PXE gene, half of their children will be
PXE carriers but none will have PXE. The upper right example "B"
brings two carriers together and on average, PXE will develop in
25% of the children; 50% will be carriers and 25% will have normal
genes. The lower example "C" illustrates the fact that if someone
with PXE marries someone with two normal genes, their children will
be carriers, but none will develop PXE.
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