4 research outputs found
A Tunisian neonatal case of co-inheritance of G6PD deficiency and HBC presenting as severe jaundice and hemolytic anemia
No full textIdentification of a mild cystic fibrosis mutation 2789+5 G to a for the first time in Tunisian population
No full textFibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization
No full textCongenital dysfibrinogenemia is a rare qualitative fibrinogen deficiency. Molecular defects that result in dysfibrinogenemia are usually caused by mutations which affect fibrinopeptide release, fibrin polymerization, fibrin cross-linking or fibrinolysis
