Summary
doi: 10.25005/2074-0581-2010-12-1-77-83
PECULIARITIES OF METABOLISM AND CORRECTING THERAPY IN CHILDREN WITH HEREDITARY HAEMOLYTIC ANEMIA
54 children with hereditary haemolytic anemia (HHA) by electro-cardio-graphical (ECG) and cytochemical methods were investigated. It was received that in 96% of children had ECG-features of mio-cardio-dystrophy. Cytochemical status of lymphocytes of peripheral blood showed inhibition of activity of enzymes of energetic metabolism - succinate dehydrogenase and ?-glicerophosphate dehydrogenase. The use of preparations of metabolic action in the complex of specific therapy leaded to increase activity of these enzymes and decrease symptoms of mio-cardio-dystrophy.
Keywords: HHA, mio-cardio-dystrophy, metabolic therapy.
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