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platelet storage pool deficiency/epistaxis
L'enllaç es desa al porta-retalls
5 resultats
Postural orthostatic tachycardia syndrome is associated with platelet storage pool deficiency.
Només els usuaris registrats poden traduir articles
Inicieu sessió / registreu-vos
Mechanisms have been postulated to explain postural orthostatic tachycardia syndrome (POTS), however, the etiology of this often debilitating disorder remains unknown. We conducted a retrospective case-control study of 181 POTS patients who exhibited/reported bleeding symptoms for a specific
Clinical and laboratory characteristics of adolescents with platelet function disorders and heavy menstrual bleeding.
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Inicieu sessió / registreu-vos
BACKGROUND
Platelet function disorders (PFDs) have emerged as an important etiology of heavy menstrual bleeding (HMB) in adolescents. However, neither clinical nor laboratory data have been methodically analyzed in this population subset. The objective of this study was to evaluate these parameters
Current Strategies in Diagnosis of Inherited Storage Pool Defects.
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Inicieu sessió / registreu-vos
Inherited platelet defects lead to bleeding symptoms of varying severity. Typically, easy bruising, petechiae, epistaxis, and mucocutaneous bleeding are observed in affected patients. The platelet defects are classified into disorders affecting either platelet surface receptors or intracellular
Management of uremic bleeding.
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Inicieu sessió / registreu-vos
The pathogenesis, clinical manifestations, and management of uremic bleeding are discussed, and the role of pharmacologic intervention in the treatment of this disorder is emphasized. Care of the patient with uremia is frequently complicated by spontaneous, life-threatening bleeding episodes.
Weak correlation of bleeding scores to platelet electron microscopy: A retrospective chart review of pediatric patients with delta-storage pool disorder.
Només els usuaris registrats poden traduir articles
Inicieu sessió / registreu-vos
BACKGROUND
Delta granule storage pool deficiency (δ-SPD) is a rare platelet disorder in which a deficiency of platelet granules leads to poor aggregation, resulting in varying clinical bleeding phenotypes. Children with δ-SPD have variable laboratory results, making the proper diagnosis and
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