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Fact Sheet

Patient Information – fact sheets and resources covering a range of blood related medical conditions, their diagnosis, treatment and management.

Haemochromatosis*

Haemochromatosis*

Haemochromatosis

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Hereditary Haemorrhagic Telangiectasia

Hereditary Haemorrhagic Telangiectasia

Hereditary Haemorrhagic Telangiectasia (HHT) – a genetic disorder characterised by abnormal connections between arteries and veins (AVMs)

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1000 563 Melbourne Haematology
Prothrombin Gene Mutation

Prothrombin Gene Mutation

Prothrombin Gene Mutation

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1000 563 Melbourne Haematology
Hereditary Spherocytosis

Hereditary Spherocytosis

Hereditary Spherocytosis or HS is a red blood cell disorder where the cells take on a shape of a ball (or sphere) instead of the normal shape of a red cell (which looks like a ‘doughnut)’. Because the red cells are in the shape of a ball they are more fragile than normal red cells. The fragile red cells can break down which is also known as red cell haemolysis and cause anaemia.

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Antiphospholipid Syndrome

Antiphospholipid Syndrome

Antiphospholipid Syndrome (APS) is a blood disorder caused by abnormal proteins (antibodies) in the blood that lead to an increase risk of blood clotting and problems with pregnancy.

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Raised Serum Ferritin

Raised Serum Ferritin

Neutropenia is the medical term for a decrease in the number of white blood cells called neutrophils.

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Patient Fact Sheet – Example 1

Patient Fact Sheet – Example 1

Ferritin is a protein that carries iron around in the blood and can be used to measure the amount of iron in the body. If the ferritin level is high, the amount of iron in the blood may also be high. If the ferritin is low, this often means the body is low in iron.

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