One of the global challenges of our time is to study the problems and preserve the biological diversity of plants. Therefore, the study of plant biodiversity in any region will always be relevant. This article presents the results of a study obtained in the course of conducting a systematic analysis of the flora of Talgar and Enbekshikazakh regions the Almaty region. It was revealed that the flora of the study area includes 114 families, of which 10 leading families make up 60.48% of the total species composition of the flora of the study area. The following families occupy the leading position in this taxonomic composition: Asteraceae (225 species, or 14.60%, 71 genus), Poaceae (132 species or 8.56%), Fabaceae-(115 species or 7.46%). The largest genera are Astragalus (44 species or 7.94%), Allium (28 species or 5.05%), Carex (27 species, 4.87%), Potentilla (23 species or 4.15%). The flora was studied with using traditional methods of floristic and geobotanical research, the main of which was route reconnaissance method. Based on the analysis of literature data, viewing of the herbarium fund of the Institute of Botany and Phytoinduction of the National Academy of Sciences of Kazakhstan, as well as their own research on the study and collection of plants in the Almaty region, a preliminary annotated list of flora was compiled, including 1541 species belonging to 554 genera and 114 families.
Inhibitory coagulopathy is a rare variant of hemorrhagic syndrome. Acquired hemophilia A is caused by the formation of inhibitors (antibodies) to Factor VIII of the blood coagulation system leading to impaired activation of the key stage of blood clotting (factor X) and development of hemorrhagic syndrome of different severity. Acquired hemophilia A is a rare disease with an incidence of 1.38-1.48 per 1 million population per year. We report a case off severe idiopathic acquired hemophilia A in a 53 year-old woman manifest as skin hemorrhages, subcutaneous and intramuscular hematomas. Hemostatic therapy described in the article resulted in the elimination of hemorrhagic syndrome and complete remission. This case represents a rare disease the knowledge of which can be useful for preventing the development of debilitating complications, and sometimes saving the patient’s life.
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