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Autor:
Hasan Mohamed A. Aal-Yaseen, Komal Sundeep Hazari, Atif Bashir Fazari, Taghrid Gergawi, Nighat Aftab
Publikováno v:
Open Journal of Obstetrics and Gynecology. :991-996
Immune thrombocytopenic purpura (ITP) is an acquired autoimmune disorder, defined by a platelet count of less than 100 × 109/L, secondary to impaired production and immune destruction of platelets. Bleeding tendency is the main presentation of this