Glucose-6-phosphate dehydrogenase (G6PD), an X-linked hereditary deficiency, is the most common of all clinically significant enzyme defects. While many drugs are responsible for haemolytic anaemia in G6PD-deficient patients, acetaminophen's imputability is still under debate, although an overdose of this drug can provoke acute haemolytic events. We report a case of a Philipino child carrying the G6PD-Vanua Lava mutation with acute haemolytic crisis related to infection in progress and acetaminophen's administration. Fever and concomitant infection, through an increment of erythrocyte glutathione depletion, sensitized the infant to the haemolytic event. In this condition, acetaminophen (or paracetamol [PCM]) was capable of inducing a haemol...
International audienceWe report the occurrence of symptomatic methemoglobinemia in a previously heal...
Seizure is a rare presentation for acute hemolysis due to G6PD deficiency. We report a previously he...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being pr...
Glucose-6-phosphate dehydrogenase (G6PD), an X-linked hereditary deficiency, is the most common of a...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited genetic disorder caused by red c...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited genetic disorder caused by red c...
Oxidative agents can cause acute haemolytic anaemia in persons with G6PD deficiency. Understanding t...
Oxidative agents can cause acute haemolytic anaemia in persons with G6PD deficiency. Understanding t...
Abstract Oxidative agents can cause acute haemolytic anaemia in persons with G6PD deficiency. Unders...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited cause of haemolytic...
SYNOPSIS Three male members of an English family with chronic haemolytic anaemia due to glucose-6-ph...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
International audienceWe report the occurrence of symptomatic methemoglobinemia in a previously heal...
Seizure is a rare presentation for acute hemolysis due to G6PD deficiency. We report a previously he...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being pr...
Glucose-6-phosphate dehydrogenase (G6PD), an X-linked hereditary deficiency, is the most common of a...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited genetic disorder caused by red c...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited genetic disorder caused by red c...
Oxidative agents can cause acute haemolytic anaemia in persons with G6PD deficiency. Understanding t...
Oxidative agents can cause acute haemolytic anaemia in persons with G6PD deficiency. Understanding t...
Abstract Oxidative agents can cause acute haemolytic anaemia in persons with G6PD deficiency. Unders...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited cause of haemolytic...
SYNOPSIS Three male members of an English family with chronic haemolytic anaemia due to glucose-6-ph...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
During a routine screening for G6PD deficiency in the Province of Matera (Southern Italy), an eleven...
International audienceWe report the occurrence of symptomatic methemoglobinemia in a previously heal...
Seizure is a rare presentation for acute hemolysis due to G6PD deficiency. We report a previously he...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being pr...