Primary Diagnosis Of Acquired Thrombocytopathy In Family Polyclinics
Keywords:
Abstract
The article is devoted to general issues of classification and differential diagnosis of thrombocytopathy. Features of pathogenesis, clinical course and diagnosis of certain rare inherited thrombocytopathies are highlighted. Particular attention is paid to the formation of the molecular basis of these diseases. The basic genetic mutations associated with a number of thrombocytopathies are given.
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References
mutation in patients with Glanzmann thrombasthenia located in the N-terminus of blade 1 of the betapropeller (Asn2Asp) disrupts a calcium binding site in blade 6. J Thromb Haemost 2011;
Raccuglia G. Grey platelet syndrome:a variety of qualitative platelet disorder. Am J Med 1971.
Gerrard J. M., Phillips D. R., Rao G. H.. Biochemical studies of two patients with the grey platelet syndrome. J Clin Invest 1980;
Levy-Toledano S., Caen J. P.,Breton-Gorius J. et al. Gray platelet syndrome: alpha-granule deficiency. Its influence on platelet function. J Lab Clin Med 1981;
Nurden A. T., Kunicki T. J., Dupuis G.et al. Specific protein and glycoprotein deficiencies in platelets isolated from two patients with the grey platelet syndrome. Blood 1982;
