haemolytic anaemia

In its severe forms, this disorder predisposes to haemolytic anaemia.

The major consequence of infection is the development of haemolytic anaemia due to the damage done to red blood cells.

The cell lyses and a haemolytic anaemia results.

Haemolytic anaemia is a characteristic sign.

Haemolytic anaemia or deficiency in red blood cells (RBCs)

Many patients with haemolytic anaemia take folic acid (vitamin B) since the greater turnover of cells consumes this vitamin.

Like primaquine, pamaquine causes haemolytic anaemia in patients with G6PD deficiency.

Association of a common dog leucocyte antigen class II haplotype with canine primary immune-mediated haemolytic anaemia.

This type of anaemia is called haemolytic anaemia and is often caused by an inherited condition, such as sickle cell anaemia.

A clinically significant haemolytic anaemia occurs only in 5-10% of sufferers, with a strong bias towards those with more severe subtypes of the disorder.

Presentation with fever, fatigue, and haemolytic anaemia requires diagnostic confirmation by identifying the parasites within red blood cells on blood film and by specific serology.

Stomatin is a 31 kDa integral membrane protein, named after the rare human haemolytic anaemia hereditary stomatocytosis.

Haemoglobinuria can be caused by haemolytic anaemia, blood transfusions, extensive burns, the bite of the recluse spider (Loxosceles), infections and strenuous exercise.

They are seen on blood films when the bone marrow is highly active in an attempt to replace red blood cell loss such as in haemolytic anaemia, haemorrhage.

It is characterized by a tower-shaped skull, dilatation of the diploe, and no signs of thalassaemia, sickle cell or other haemolytic anaemia.

With chronic haemolysis - the individual has a moderate to severe symptomatic haemolytic anaemia (this subtype has variable penetrance in some pedigrees)

Dehydrated HSt (hereditary xerocytosis; hereditary hyperphosphatidylcholine haemolytic anaemia)

The disease presents with exercise-induced muscle cramps and weakness (sometimes rhabdomyolysis), myoglobinuria, as well as with haemolytic anaemia causing dark urine a few hours later.

Similarly to the spectrin mutations, band 4.1 mutations cause a mild haemolytic anaemia in the heterozygous state, and a severe haemolytic disease in the homozygous state.

Rarely CNS toxicity including convulsions (especially with high doses or in severe renal impairment), interstitial nephritis, haemolytic anaemia, leucopenia, thrombocytopenia, and coagulation disorders.

In his clinical role, Woodruff started a vascular surgery program and worked with the use of immunotherapy as a cancer treatment as well as the treatment of autoimmune haemolytic anaemia.

Due to the risk of a risk of haemolytic anaemia, the U.S. Food and Drug Administration (FDA) withdrew approval for nomifensine on March 20, 1992.

It is a unique glycolytic enzymopathy that is characterized by chronic haemolytic anaemia, cardiomyopathy, susceptibility to infections, severe neurological dysfunction, and, in most cases, death in early childhood.

The research group's principal investigations concerned immunological tolerance (the body's acceptance of tissues, as opposed to rejection), autoimmune haemolytic anaemia (especially in mice), and immune responses to cancer in various animals.

Neonates (babies up to the age of one month) have immature enzyme systems in their red blood cells (glutathione instability) and nitrofurantoin must therefore not be used because it can cause haemolytic anaemia.