Estudio de la influencia de la adherencia y los niveles plasmáticos de factor en las comorbilidades, complicaciones y consecuencias de la hemofilia
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2025
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15/07/2024
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Universidad Complutense de Madrid
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Abstract
Las coagulopatías congénitas (CC) son trastornos hereditarios de la hemostasia caracterizados por el déficit total o parcial de alguna proteína que participa en el proceso de coagulación. Son la hemofilia A o déficit de factor VIII, hemofilia B o déficit de Factor IX, enfermedad de Von Willebrand con déficit del factor de Von Willebrand y otras patologías que presentan déficit de otros factores como el VII, X, etc. Estas patologías se caracterizan por episodios hemorrágicos que pueden ser espontáneos o producirse tras traumatismos. Las hemorragias más frecuentes, hasta un 80%, afectan al aparato locomotor y el resto a otras localizaciones como digestivas, sistema nervioso central, etc. Las hemorragias más habituales son las articulares y musculares. Las hemorragias repetidas dan lugar a artropatías altamente invalidantes. Las hemorragias localizadas en otras partes del organismo son menos frecuentes, pero de mayor gravedad...
Congenital coagulopathies (CC) are hereditary disorders of hemostasis characterized by total or partial deficiency of a protein involved in the coagulation process. They are hemophilia A or coagulation factor VIII deficiency, hemophilia B or Factor IX deficiency, Von Willebrand's disease with Von Willebrand's factor deficiency and other pathologies that present deficiency of other factors such as VII, X, etc. With the exception of Von Willebrand's disease, all of them are rare diseases.These pathologies are characterized by hemorrhagic episodes that can be spontaneous or occur after trauma. The most frequent hemorrhages, up to 80%, affect the musculoskeletal system and the rest affect other locations such as the digestive tract, central nervous system, etc. These pathologies are characterized by hemorrhagic episodes that can be spontaneous or occur after trauma. The most frequent hemorrhages, up to 80%, affect the musculoskeletal system and the rest affect other locations such as the digestive tract, central nervous system, etc...
Congenital coagulopathies (CC) are hereditary disorders of hemostasis characterized by total or partial deficiency of a protein involved in the coagulation process. They are hemophilia A or coagulation factor VIII deficiency, hemophilia B or Factor IX deficiency, Von Willebrand's disease with Von Willebrand's factor deficiency and other pathologies that present deficiency of other factors such as VII, X, etc. With the exception of Von Willebrand's disease, all of them are rare diseases.These pathologies are characterized by hemorrhagic episodes that can be spontaneous or occur after trauma. The most frequent hemorrhages, up to 80%, affect the musculoskeletal system and the rest affect other locations such as the digestive tract, central nervous system, etc. These pathologies are characterized by hemorrhagic episodes that can be spontaneous or occur after trauma. The most frequent hemorrhages, up to 80%, affect the musculoskeletal system and the rest affect other locations such as the digestive tract, central nervous system, etc...
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Tesis inédita de la Universidad Complutense de Madrid, Facultad de Farmacia, leída el 15/07/2024