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Pyruvate kinase deficiency

Disease Pyruvate kinaseQ fever

Pyruvate kinase deficiency
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Pyroglutamic Aciduria
Pyroglutamicaciduria
Pyrroline Carboxylate Dehydrogenase Deficiency
Pyrroloporphyria
Pyruvate Carboxylase Deficiency
Pyruvate Dehydrogenase Deficiency
Pyruvate Kinase Deficiency ...

Pyruvate Kinase Deficiency
In this condition, the body is missing an enzyme called pyruvate (PI-ru-vate) kinase. Not having enough of this enzyme causes red blood cells to break down easily.

Definition Pyruvate kinase deficiency (PKD) is part of a group of disorders called hereditary nonspherocytic hemolytic anemias. Hereditary nonspherocytic anemias are rare genetic conditions that affect the red blood cells.

Red Cell Pyruvate Kinase Deficiency in…
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[Hereditary Spherocytic Hemolytic… ...

Do you have close relatives who have sickle cell anemia, thalassemia, pyruvate kinase deficiency, glucose-6-phosphate deficiency or another form of inherited anemia?
What medications do you take?

Common examples are pyruvate kinase deficiency (see Anemias Caused by Hemolysis: Embden-Meyerhof Pathway Defects) and glucose-6-phosphate dehydrogenase (G6PD) deficiency (see Anemias Caused by Hemolysis: Glucose-6-Phosphate Dehydrogenase (G6PD) ...

Pyruvate kinase deficiency a hereditary deficiency of the enzyme pyruvate kinase. Pyruvate kinase deficiency results in hemolytic anemia. Quartile one fourth of a sample or population. Quintile one fifth of a sample or population.

Infection
Prematurity
Pyruvate kinase deficiency
Transfusions
The following interfere with the body's ability to process and remove bilirubin: ...

MODY 2/HHF3 Â- GSD type VII, Tarui's, phosphofructokinase Â- Triosephosphate isomerase deficiency Â- Pyruvate kinase deficiency
Gluconeogenesis
PCD Â- Fructose bisphosphatase deficiency Â- GSD type I, von Gierke, glucose 6-phosphatase ...

The more common of the enzyme deficiencies that lead to HNSHA involve glucose-6-phosphate dehydrogenase (G6PD) deficiency, pyruvate kinase deficiency and hexokinase deficiency.

determined defects include defects of the membrane (as in hereditary spherocytosis), defects in the structure or production of hemoglobin (as in sickle cell anemia or thalassemia), or deficiencies of needed enzymes (as in pyruvate kinase deficiency).

See also: Pyruvate kinase, Deficiency, Anemia, Hemolytic anemia, Infections

Disease Pyruvate kinaseQ fever

 
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