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anémie hémolytique congénitale

Increased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency AbstractTriosephosphate isomerase deficiency is associated with the accumulation of dihydroxyacetonephosphate (DHAP) to abnormally high levels, congenital haemolytic anaemia and a clinical syndrome of progressive neuromuscular degeneration leading to infant mortality....

général - core.ac.uk -

Hereditary xerocytosis due to mutations in piezo1 gene associated with heterozygous pyruvate kinase deficiency and beta-thalassemia trait in two unrelated families... It is sometimes misdiagnosed as hereditary spherocytosis or other congenital haemolytic anaemia....

PDF: air.unimi.it

Haemolytic anaemia with acute renal disease by... The earliest reports were by Hensley (1952), who described 3 patients with glomerulonephritis complicated by haemolytic anaemia, and by Dacie, Mollison, Richardson, Selwyn, and Shapiro (1953), whose patient with atypical congenital haemolytic anaemia ' was found at necropsy to have nephritis'....

PDF: adc.bmj.com

Congenital haemolytic anaemia associated with abnormal inducible red cell cation permeability.Congenital haemolytic anaemia in a 14 year old girl was caused by increased red cell membrane cation permeability....

PDF: www.pubmedcentral.nih.gov

Atypical congenital haemolytic anaemia byThe most common type of congenital haemolytic anaemia found in Great Britain is familial haemo-lytic anaemia (chronic acholuric jaundice)....

PDF: adc.bmj.com