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Braz. j. med. biol. res ; 24(2): 133-9, 1991. tab
Article in English | LILACS | ID: lil-99446

ABSTRACT

A 27 year old Brazilian male of both Portuguese and Spanish origin presenting nonspherocytic chronic hemolytic anemia was found to have a rare glucose-6-phosphate dehydrogenase variant herein named Gd(-) Carapicuiba. The red blood cell enzyme variant is characterized by a moderate enzyme deficiency (47%), high Km for its substrates G6P and NADP, decreased activity against deamino-NADP, increased Ki for NADPH and decreased heat stability. The clinical signs of the patient are probably related to these properties of the enzyme variant


Subject(s)
Adult , Humans , Male , Anemia, Hemolytic, Congenital Nonspherocytic/enzymology , Erythrocytes/enzymology , Glucosephosphate Dehydrogenase Deficiency/enzymology , Glucosephosphate Dehydrogenase/genetics , Anemia, Hemolytic, Congenital Nonspherocytic/complications , Genetic Variation , Glucosephosphate Dehydrogenase Deficiency/complications , Glucosephosphate Dehydrogenase/blood , Hemolysis , Pedigree
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