G6PD deficiency

G6PD deficiency

abbreviation for glucose-6-phosphate dehydrogenase deficiency. G6PD is an enzyme in the pentose-phosphate shunt of the Embden-Meyerhof pathway.

G6PD deficiency

 Glucose-6-phosphate dehydrogenase deficiency, see there.

Glucose-6-phosphate dehydrogenase (G6PD) deficiency

An inherited disorder in which the body lacks an enzyme that normally protects red blood cells from toxic chemicals. When people with this condition take certain drugs, their red blood cells break down, causing anemia. This may also happen when they have a fever or an infection. The condition usually occurs in males. About 10% of black males have it, as do a small percentage of people from the Mediterranean region.
References in periodicals archive ?
However, breastfeeding an infant with G6PD deficiency could lead to hemolytic anemia.
77pc had G6PD deficiency, an inherited glucose deficiency that affects functions of red blood cells, while a slight increase in the prevalence of other genetic diseases was registered.
Early phagocytosis of glucose-6-phosphate dehydrogenase (G6PD) deficient erythrocytes parasitized by Plasmodium falciparium may explain malaria protection in G6PD deficiency.
According to UAE GDA, the most common genetic disorders in UAE include thalassemia, sickle cell anaemia, haemophilia, G6PD deficiency and cystic fibrosis.
However, Aspirin can be used with caution in G6PD deficiency, breast feeding, chronic or recurrent peptic ulcer, severe renal or hepatic damage.
Neonates with congenital anomalies and syndromes, Rh incompatibility and G6PD deficiency were excluded.
Pencil cells Iron deficiency Stomatocytes Artifact (due to slow drying in humid environment), Liver disease, alcoholism, Rh-null disease, Obstructive lung disease Elliptocytes Hereditary Elliptocytosis (>25%) Bite cells (degmacytes) G6PD deficiency, Oxidative stress, unstable haemoglobins, congenital heinz body anaemia Basket cells (half ghost Oxidant damage, G6PD deficiency, cells/Blister cells) Unstable haemoglobins Spherocytes Hereditary spherocytosis, ABO incompatibility, Autoimmune hemolytic anemia (warm antibody type), Severe burns Teardrop red cell Idiopathic myelofibrosis, (dacrocytes, myelophthisic anaemia, lacrymocytes) thalassemias
The most common genetic blood disorder in the Omani society is the G6PD deficiency as 28% of males and 12% of females have the gene of the disease.
In active G6PD deficiency, Heinz bodies can be seen in red blood cells on a blood film, liver enzymes (to exclude other causes of jaundice) and Lactate dehydrogenase (elevated in hemolysis and a marker of hemolytic severity).
Hemolytic anemia after voluntary ingestion of henna (Lawsonia inermis) decoction by a young girl with G6PD deficiency.
5] The aim of this study was to find out the prevalence of frequency of sickle cell disease, G6PD deficiency, and [alpha] and [beta] thalassemia in healthy tribal medical students and to increase their own awareness about the disease they are experiencing and increase sensitization toward social awareness.