Hemophilia is an inherited X-linked coagulopathy defined by a deficiency or abnormality in the clotting function of factor VIII (Hemophilia A) IX B). Prophylaxis – regular administration therapeutic products to maintain hemostasis and prevent bleeding mainstream treatment. Addressing development scientific evidence for administrating prophylaxis goal this review. modality choice people with sev...

From an estimated population of 2500 sian and three had underlying congenital hemophiliacs seen between 1965 and anomalies. No etiology was apparent in 976, 71 with documented central ncr38%. Sixty-five patients had intracranial vous system (CNS) bleeding were studied bleeding. Those with intracerebral bleeding retrospectively: 56 had factor VIII deficiency had a poorer prognosis than did those...

Introduction Cerebral venous sinus thrombosis (CVST), although a common diagnosis, is missed frequently by both general practitioners and neurologists. The most common presenting complaints are headache with focal neurological symptoms such as weakness, numbness, and aphasia. CVST has a female predominance of 3:1. A risk factor usually is able to be determined, most common of which is oral cont...

is a congenital, often familial, hemorrhagic disorder which was distinguished from classical hemophilia (AHG deficiency, factor VIII deficiency, hemophilia A) in 1952.13 Like the latter, it is usually inherited as a sex-linked recessive trait: only the male hemizygote for the abnormal gene is clinically affected, and the female heterozygote or carrier is asymptomatic. From a eugenic standpoint ...