A young male presented to us with the chief complaints of jaundice, non-bilious vomiting and intermittent high-grade fever in the background of past history of recurrent blood transfusions.On examination, he had pallor, icterus with a massive non tender splenomegaly and his laboratory parameters were suggestive of indirect hyperbilirubinemia with low haptoglobin and elevated lactate dehydrogenase levels with reticulocytosis and erythroid hyperplasia on bone marrow aspiration. His Direct and indirect coombs test were negative.To rule out hemoglobinopathies, his hemoglobin electrophoresis was sent, which turned out to be normal. Hence, red blood cell membrane and enzyme studies were carried out which revealed Glucose-6-phosphate isomerase def...
The frequency of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency was determined in 54 male pat...
Glucose-6-phosphate dehydrogenase (G6PD) is the first enzyme of the pentose phosphate pathway, provi...
Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency is an X-linked genetic disorder associated with ...
A glucose-6-phosphate isomerase deficiency is described in an Arab boy suffering from chronic hemoly...
Glucose-6-phosphate isomerase (GPI, EC 5.3.1.9) is a dimeric enzyme that catalyzes the reversible is...
Glucose-6-phosphate isomerase (GPI, EC 5.3.1.9) is a dimeric enzyme that catalyzes the reversible is...
Hereditary hemolytic anemia associated with glucose phosphate isomerase (GPI) deficiency was first r...
The first two mutations causing hereditary glucose-6-phosphate isomerase (GPI) deficiency associated...
Deficiency of glucose-6-phosphate dehydrogenase (G6PD) is the commonest enzyme deficiency in humans ...
SYNOPSIS Three male members of an English family with chronic haemolytic anaemia due to glucose-6-ph...
A rare case of hereditary erythrocyte enzymopathy, namely 6-phosphogluconate dehydrogenase (6PGD) de...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being pr...
PubMedID: 2267926Clinical and laboratory evaluation of 60 boys with hemizygous, 12 girls with homozy...
Molecular, kinetic, and functional studies were carried out on erythrocytes and leukocytes in a Span...
A 54-year-old Chinese male hepatitis B virus (HBV) carrier presented with jaundice, cyanosis, and co...
The frequency of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency was determined in 54 male pat...
Glucose-6-phosphate dehydrogenase (G6PD) is the first enzyme of the pentose phosphate pathway, provi...
Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency is an X-linked genetic disorder associated with ...
A glucose-6-phosphate isomerase deficiency is described in an Arab boy suffering from chronic hemoly...
Glucose-6-phosphate isomerase (GPI, EC 5.3.1.9) is a dimeric enzyme that catalyzes the reversible is...
Glucose-6-phosphate isomerase (GPI, EC 5.3.1.9) is a dimeric enzyme that catalyzes the reversible is...
Hereditary hemolytic anemia associated with glucose phosphate isomerase (GPI) deficiency was first r...
The first two mutations causing hereditary glucose-6-phosphate isomerase (GPI) deficiency associated...
Deficiency of glucose-6-phosphate dehydrogenase (G6PD) is the commonest enzyme deficiency in humans ...
SYNOPSIS Three male members of an English family with chronic haemolytic anaemia due to glucose-6-ph...
A rare case of hereditary erythrocyte enzymopathy, namely 6-phosphogluconate dehydrogenase (6PGD) de...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being pr...
PubMedID: 2267926Clinical and laboratory evaluation of 60 boys with hemizygous, 12 girls with homozy...
Molecular, kinetic, and functional studies were carried out on erythrocytes and leukocytes in a Span...
A 54-year-old Chinese male hepatitis B virus (HBV) carrier presented with jaundice, cyanosis, and co...
The frequency of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency was determined in 54 male pat...
Glucose-6-phosphate dehydrogenase (G6PD) is the first enzyme of the pentose phosphate pathway, provi...
Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency is an X-linked genetic disorder associated with ...