What is Hemolytic Anemia associated with a deficiency of glucose-6-phosphate dehydrogenase (G-6-FDG)? Hemolytic anemia associated with a deficiency of glucose-6-phosphate dehydrogenase (G-6-FDG) is a hereditary hemolytic anemia associated with a deficiency of enzyme activity. In
Continue readingWhat is Hairy Cell Leukemia? Hairy-cell leukemia is a rare variant of chronic leukemia, which is considered an independent nosological unit and is currently not considered as one of the clinical and morphological variants of
Continue readingWhat is the Rando-Osler Disease? Rando-Osler disease is the most common hereditary hemorrhagic vasopathy with focal thinning of the walls and expansion of the microvascular lumen, with inadequate local hemostasis. This pathology is inherited by
Continue readingWhat is Markiafavi-Micheli Disease? Markiafavi-Micheli’s disease is a rather rare form of acquired hemolytic anemia, characterized by a violation of the structure of erythrocytes, neutrophils and platelets, accompanied by signs of intravascular erythrocyte destruction. An
Continue readingWhat is Christmas Disease? The term “hemophilia B” is understood as a hereditary hemorrhagic diathesis, characterized by a deficiency in the activity of the plasma component of thromboplastin (factor IX). For the first time, hemophilia
Continue readingWhat is Von Willebrand Disease? The disease was first studied in 1926 by the scientist Willebrand, who on the Aland Islands described a family with a kind of autosomal dominantly inherited hemorrhagic diathesis, similar to
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