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Pyruvate kinase

Disease Pyruvate dehydrogenase deficiencyPyruvate kinase deficiency

Pyruvate kinase deficiency
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M Type Pyruvate Kinase
Medical Dictionary
Definition of medical terminology for M Type Pyruvate Kinase.

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.

Serum Pyruvate Kinase; Simultaneous Pancreas-kidney [transplantation]; Superficial Punctate Keratitis
TINU
Tubulo-interstitial Nephritis-uveitis [syndrome] ...

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…
Related Articles Red cell pyruvate kinase deficiency in Southern Sardinia. Blood… more…
[Hereditary Spherocytic Hemolytic… ...

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.

L Type Pyruvate Kinase
L Type VDCC
L Type VDCC alpha 1 Subunit
L Type VDCC alpha 2 Subunit
L Type VDCC beta Subunit
L Type VDCC delta Subunit
L Type VDCC gamma Subunit
L Type Voltage Dependent Calcium Channels
L Tyrosine
L Valine ...

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) ...

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 ...

Hemolytic Anemias Due to Enzyme Deficiency, Other; Hemolytic Nonspherocytic (Hereditary), Type II, Hexokinase Deficiency, Pyruvate Kinase [PK] Deficiency, Triosephosphate Isomerase Deficiency
282.4 -
Thalassemia ...

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

Ptyalography
Pulmonary angiography
Pulmonary arteriography
Pulmonary function tests
Pulmonary ventilation/perfusion scan
Pulse
Punch biopsy
Purified protein derivative standard
Pyruvate kinase ...

See also: Deficiency, Anemia, Hemolytic anemia, Cancer, Pyruvate kinase deficiency

Disease Pyruvate dehydrogenase deficiencyPyruvate kinase deficiency

 
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