W. A. Shokunbi, O. W. Aworanti, P. O. Olatunji, M. D. Dairo, E. S. Fakunle, O. T. Ojo, Saleh Yuguda, Leke Ibijola, Kapona Iwara, C. I. Ajuba & F. A. Fehintola·Asian Journal of Medicine and Health·2023
Introduction: Haemophilia is a rare inherited bleeding disorder that affects predominantly male because it is an X chromosome linked disorder. The severity of the disease is determined by the percentage of Factors VIII and IX activity in the individuals with Haemophilia. Objectiv...
Open access
Research Article10.9734/ajmah/2023/v21i11920
Background: Hydroxyurea (HU) has redefined the quality of life of children with sickle cell anaemia and their care givers. Despite the acclaimed benefits of HU, the drug could be associated with variable side effects affecting different systems in the human body, including the sk...
Open access
Research Article10.9734/ijmpcr/2019/v12i130097
Introduction/Aim: Haemophilia is a rare X chromosome linked inherited bleeding disorder, characterized by deficiency of coagulation factor VIII in Haemophilia A or factor IX in Haemophilia B. Patients deficient of either of these coagulation factors are prone to fracture as a res...