Bleeding Disorders Glossary
AIDS. Acquired Immune Deficiency Syndrome.
A disease caused by a breakdown in the immune system (which defends
us from germs) that follows when someone has become infected with human
immunodeficiency virus (HIV).
Arteries. Blood vessels that carry blood
from the heart and lungs to other parts of the body.
Blood vessels. Tubes that carry
blood to cells in all parts of the body.
Bruise. A black and blue mark under the
surface of the skin, caused by bleeding under the skin.
Capillaries. The smallest blood vessels
that reach into the tiniest areas of the body.
Carrier. A person whose body carries
a gene with the information that transmits a certain characteristic,
but who does not show that characteristic.
Cartilage. A tough, elastic substance
that covers and protects the bone ends in many movable joints.
Cell. The smallest unit of living tissue
capable of functioning independently. All human life starts as a single
cell inside the mother.
Chromosome. A structure made up of
genes, located in each cell.
Clot. A plug that develops to stop the body
from bleeding.
Clotting factors. 1. Proteins
made by the body that act as a team to relay the message to make a fibrin
net. There are at least 14 clotting factors, identified by roman numerals.
A deficiency in one of the clotting factors causes prolonged bleeding
and is known as hemophilia. 2. Medicine made from human blood sources,
or derived from genes, that replaces the missing clotting factor in
people with hemophilia, allowing their blood to clot successfully.
Deficiency. Lacking something that
belongs or is needed.
Enzymes. Substances (proteins) in the
blood that break down tissue. When enzymes break down old blood pooled
in a joint following a joint bleed, they clean up the joint but also
may damage normal tissue such as cartilage.
Factor. Medicine used to stop bleeding
in people with hemophilia. Also known as factor concentrate, or clotting
factor, it is infused directly into the bloodstream.
Factor VIll deficiency.
A blood disorder in which a person is lacking or has nonfunctioning
factor VIII in the blood, causing prolonged bleeding. Also known as
hemophilia A, or classical hemophilia.
Factor IX deficiency. A
blood disorder in which a person is missing or has nonfunctioning factor
IX in the blood, causing prolonged bleeding. Also known as hemophilia
B, or "Christmas" disease.
Fibrin.A protein
that appears as a tangle of threads, created by the blood's clotting
factors. Fibrin acts like a net to hold a platelet plug over a torn
blood vessel wall in order to form a clot and stop bleeding.
Gene.A bundle
of chemical information that lies on the chromosomes. Contains chemical
information that tells the body how to develop. Genes also carry the
directions for blood clotting.
Genetics.The
study of the transmission of characteristics from parent to child through
genes.
Gene therapy.Using or altering genes to help cure diseases.
Hemophilia.A
blood disorder characterized by prolonged bleeding, and the inability
of the blood to clot properly.
Immune system.The part of the body responsible for defending it against invading
foreign substances including germs, bacteria and viruses.
Infuse. To inject a substance directly
into the veins.
Inherit. To receive physical characteristics
from the parents through the genes.
Inhibitor. A blood protein that destroys
or "inhibits" factor VIII when it is infused into the bloodstream,
making it useless.
Joint. A place, where two bones meet, that
allows movement.
Joint cavity. The space created
where two bones meet in a joint.
Mild hemophilia. A type of hemophilia
in which 5% to 40% of a specific blood factor works successfully. Characterized
by infrequent bleeding, sometimes after only severe injuries or surgery.
Moderate hemophilia. A type
of hemophilia in which 1% to 4% of a specific blood factor works successfully.
Characterized by bleeding after injury.
Myths. Stories, legends or invented explanations
that are retold so often that they are accepted as truth.
Plasma. The clear, yellowish liquid part
of the blood that contains the clotting factors.
Platelets. Donut-shaped substances
in the blood that stick together and help plug a torn blood vessel to
stop bleeding.
Prophylaxis. Prevention. In hemophilia,
infusing with clotting factor regularly to prevent bleeds from occurring.
Proteins. Microscopic substances in
the body, responsible for all growth and maintenance of living tissue.
Red blood cells. Blood cells
that carry food and oxygen to all cells in the body.
Scab. A dried-up blood clot on the surface
of the skin.
Severe hemophilia. A type of
hemophilia in which less than 1% of a specific blood factor works. Characterized
by frequent and spontaneous bleeding.
Sex chromosomes. One of the 23
pairs of chromosomes in each cell, denoted as XX or XY, that determines
whether the organism will be a female or male.
Spontaneous bleeding. Bleeding
that appears to have no direct cause.
Symptoms. Physical or behavioral signs
of a suspected injury or disease.
Target joint. A joint that has repeated
bleeds with eventual signs of damage.
Veins. Blood vessels that carry blood lacking
oxygen and food back to the heart and lungs.
White blood cells. Colorless
blood cells that help protect the body from foreign particles and bacteria
by destroying them.
XX. A chromosome pair that determines a baby's
sex as female.
XY. A chromosome pair that determines
a baby's sex as male.