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institute of
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on the other end of the spectrum
Bleeding disorders such as hemophilia and von
Willebrand disease result when the blood lacks
certain clotting factors. These diseases are
almost always inherited, although in rare cases
they can develop later in life if the body forms
antibodies that fight against the blood's natural
clotting factors.Individuals and pregnant women
with a family history of bleeding disorders
should talk to their doctors about detection and
treatment. Symptoms of bleeding disorders may
include:
Easy bruising
Bleeding gums
Heavy bleeding from small cuts or dental work
Unexplained nosebleeds
Heavy menstrual bleeding
Bleeding into joints
Excessive bleeding following surgery
factors and conditions leading to inadequate clothing
Hemophilia (a)
hemophilia (b) inherited
Hemophilia (c)
Vitamin K deficiency
Hemophilia
Hemophilia is a rare, inherited bleeding disorder
that can range from mild to severe, depending on
how much clotting factor is present in the blood.
Hemophilia is classified as type A or type B, based
on which type of clotting factor is lacking (factor
VIII in type A and factor IX in type B). Hemophilia
results from a genetic defect found on the X
chromosome. Women have two X chromosomes. Women
who have one X chromosome with the defective gene
are termed carriers and they can pass the disease
onto their sons. Due to random chromosome
activation, some women carriers may range from
asymptomatic to symptomatic depending on how
much of their factor VIII or IX is inactivated. In
fact, some women may have “mild hemophilia,”
though this is less common. Men have one X and one Y
chromosome, so if their X chromosome has the
defective gene, they will have hemophilia.
Von-Willebrand disease
Von Willebrand disease (VWD) is a blood disorder in
which the blood does not clot properly. Blood contains
many proteins that help the blood clot when needed.
One of these proteins is called von Willebrand factor
(VWF). People with VWD either have a low level of VWF in
their blood or the VWF protein doesn’t work the way it
should.
Normally, when a person is injured and starts to bleed,
the VWF in the blood attaches to small blood cells
called platelets. This helps the platelets stick
together, like glue, to form a clot at the site of injury
and stop the bleeding. When a person has VWD, because
the VWF doesn’t work the way it should, the clot might
take longer to form or form incorrectly and bleeding
might take longer to stop. This can lead to heavy, hard-
to-stop bleeding. Although rare, the bleeding can be
serious enough to damage joints or internal organs, or
even be life-threatening.
Vitamin K deficiency
Vitamin K is important because it helps the liver make
proteins that allow your blood to clot normally, to prevent
excessive bleeding. It is also important for healthy bones.
Adults usually have enough vitamin K, because normal
bacteria in the gut produce it. It is also in the fat of much of
the food that we eat. Vitamin K gets stored in the liver, so
you don’t need to eat it every day, unlike some other
vitamins.Not having enough vitamin K in the body makes you
more likely to bleed. You may bruise more easily than usual,
or it may be more difficult to stop bleeding after an injury
or surgery.Vitamin K deficiency in healthy adults is rare.
Most adults with vitamin K deficiency have a serious health
problem such as:
cystic fibrosis
digestive disorders that cause fat malabsorption
a blocked bile duct
taking anticoagulants, such as warfarin
People taking antibiotics for long periods of time are also
more likely to develop vitamin K deficiency.