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Glucose-6-phosphate dehydrogenase deficiency

Disease Glucose tolerance testGlucose-galactose malabsorption

Glucose-6-phosphate dehydrogenase deficiency
Definition
Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency is a hereditary condition in which red blood cells break down when the body is exposed to certain drugs or the stress of infection.

 


Glucose-6-Phosphate Dehydrogenase Deficiency Causes, Symptoms and Treatment and Related Disorders ...

Glucose-6-phosphate dehydrogenase deficiency
Alternate Names : G-6-PD deficiency, Hemolytic anemia due to G6PD deficiency, Anemia - hemolytic due to G6PD deficiency
Definition ...

What is glucose-6-phosphate dehydrogenase deficiency?
Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that occurs most often in males.

G6PD deficiency (Glucose-6-Phosphate Dehydrogenase Deficiency)
What is G6PD deficiency?
Who gets G6PD deficiency?
Predisposing Factors
Progression
Probable Outcomes
How is G6PD deficiency Diagnosed?
How is G6PD deficiency treated?

glucose-6-phosphate dehydrogenase deficiency (G6PD) - a deficiency of an enzyme (G6PD) in red blood cells, causing hemolytic anemia.
gluten - a protein found in wheat, rye, barley, and oats.

Glucose-6-phosphate dehydrogenase deficiency (G6PD) - an inherited disease in which a deficiency of the enzyme G6PD affects red blood cells and can cause hemolytic anemia.
Gluten - a protein found in wheat, rye, barley, and oats.

Glucose-6-phosphate dehydrogenase deficiency
Heart attack
Hemolytic anemia ...

Glucose-6-phosphate dehydrogenase deficiency
Idiopathic aplastic anemia
Idiopathic autoimmune hemolytic anemia ...

glucose-6-phosphate dehydrogenase deficiency (G6PD),
drugs or other toxins, and
autoimmune disorders.

Definition Glucose-6-phosphate dehydrogenase deficiency is an inherited condition caused by a defect or defects in the gene that codes for the enzyme, glucose-6-phosphate dehydrogenase (G6PD).

Related Articles Glucose-6-phosphate dehydrogenase deficiency. Lancet. 2008 Jan 5;371… more…
Clinical Trial
No clinical trials found ...

inherited conditions, such as sickle cell disease, thalassemia, and glucose-6-phosphate dehydrogenase deficiency
autoimmune disorders, conditions in which a person's immune system attacks his or her own body.

Glucose-6-Phosphate Dehydrogenase Deficiency ... darkened urine
Glutaric aciduria 2 ... glycosuria
Gnathostoma hispidum infection ... blood in urine
Gnathostoma Infection ... blood in urine
Gnathostoma spinigerum infection ... blood in urine ...

Officially, favism is known as Glucose-6-Phosphate Dehydrogenase Deficiency, or G6PD.

Glucose-6-Phosphate Dehydrogenase Deficiency
Glucose-Galactose Malabsorption
Glucose-Galactose Malabsorption
Glucosyl cerebroside lipidosis
Glucosylceramidase deficiency
Glutaric Acidemia I
Glutaric Acidemia II
Glutaric Aciduria I ...

glucose-6-phosphate dehydrogenase deficiency), closer follow-up for blood hemoglobin levels and reticulocyte counts should be implemented (see [#section-6 PRECAUTIONS]).

Glucose-6-phosphate dehydrogenase deficiency
Feeding tube insertion - gastrostomy
Focal segmental glomerulosclerosis
Sodium - urine
Inborn errors of metabolism
Hereditary urea cycle abnormality
Paroxysmal supraventricular tachycardia (PSVT) ...

implantable cardiac Deficiency diseases Deficiency, adenosine deaminase (ADA) Deficiency, ankyrin Deficiency, ceruloplasmin Deficiency, FALDH Deficiency, GALT Deficiency, glucocerebrosidase Deficiency, glucose-6-phosphate dehydrogenase Deficiency, ...

Glucose-6-phosphate dehydrogenase deficiency
Glucosylceramidase deficiency
Glucuronyl transferase deficiency (type I Crigler-Najjar)
Glue ear
Glutamate-induced asthma
Gluten intolerance
Gluten-sensitive enteropathy ...

See also: Deficiency, Symptom, Anemia, Hemolytic anemia, Pregnancy

Disease Glucose tolerance testGlucose-galactose malabsorption

 
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