Diagnostic problems in severe neonatal jaundice and G6PD deficiency in Greece

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3114167 9 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Diagnostic problems in severe neonatal jaundice and G6PD deficiency in Greece
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Examinations were made of 302 full-term newborn infants with severe jaundice (indirect bilirubin >20 mg./100 ml. in 79.7% of the cases) for G6PD deficiency by 3 diagnostic methods, of which the methaemoglobin-elution test proved to be superior. 99 or 32.7% of the cases were found to be G6PD deficient by the latter method (59 males and 40 females): a male : female ratio of 1.47. 8 of the 59 males had normal values of G6PD activity and are probably cases of the mild G6PD deficiency type. The difficulties involved in the diagnosis of G6PD deficiency in the newborn period were discussed.
Έτος δημοσίευσης:
1968
Συγγραφείς:
Zannos-Mariolea, L.
Thomaidis, Th.
Georgizas, G.
Gavrielidou, E.
Benetos, S.
Περιοδικό:
Archives of Disease in Childhood
Εκδότης:
BMJ Publishing Group
Τόμος:
43
Αριθμός / τεύχος:
227
Σελίδες:
36-41
Λέξεις-κλειδιά:
diagnostic agent; glucose 6 phosphate dehydrogenase; glutathione; methemoglobin, article; comparative study; erythrocyte; female; glucose 6 phosphate dehydrogenase deficiency; Greece; human; male; newborn; newborn jaundice, Comparative Study; Erythrocytes; Female; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glutathione; Greece; Human; Infant, Newborn; Jaundice, Neonatal; Male; Methemoglobin
Επίσημο URL (Εκδότης):
DOI:
10.1136/adc.43.227.36
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.