loading

Haemostatic disorders in nonsplenectomized and splenectomized thalassaemic children / Shebl, S.;El Sharkawy, H.M.;El Fadaly, N.H.

Tác giả : Shebl, S.;El Sharkawy, H.M.;El Fadaly, N.H.

Năm xuất bản : 1999

Chủ đề : 1. Antithrombin III. 2. Bleeding Time. 3. Ferritins. 4. Hemorrhagic Disorders. 5. Liver Function Tests. 6. Platelet Aggregation. 7. Platelet Count. 8. Protein C. 9. Splenectomy. 10. Thalassemia. 11. Thrombosis.

Thông tin chi tiết

Tóm tắt :

1171-1177 A group of 40 thalassaemic patients [20 splenectomized and 20 nonsplenectomized] from the Haematology Unit of Tanta University Hospital [age range: 3-14 years] were studied to identify the mechanisms by which haemorrhagic and thrombotic complications occur in thalassaemic patients. The patients' levels of protein C, antithrombin III and in vitro platelet aggregation in response to collagen were compared with those of 20 controls. The study suggests that thrombocytosis, increased platelet aggregation and decreased natural coagulation inhibitors [protein C and antithrombin III] in splenectomized thalassaemic children may be significant in thrombotic complications in such patients. Defective platelet aggregation and prothrombin activity in nonsplenectomized children may also give rise to haemorrhagic tendencies

 Thông tin dữ liệu nguồn

 Thư viện  Ký hiệu xếp giá  Dữ liệu nguồn
Tổ chức y tế thế giới
https://iris.who.int/handle/10665/118813