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Treatment of spontaneous intracerebral haemorrhage in Glanzmann's thrombasthenia

✍ Scribed by P. Vigren; J. O. Ström; P. Petrini; M. Callander; A. Theodorsson


Book ID
114729076
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
120 KB
Volume
18
Category
Article
ISSN
1351-8216

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Glanzmann Thrombasthenia, an exceptional inherited platelet disorder is characterized by a complete lack of platelet aggregation due to a defect in the alpha(IIb)beta(3) complex or to a qualitative abnormality of this complex. Advances in molecular biology have permitted to precise the molecular abn

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## Abstract ## Objectives/Hypothesis: To understand Glanzmann's thrombasthenia and provide insight to the management of epistaxis in children with this disease. ## Study Design: Retrospective chart review. ## Methods: All children diagnosed with Glanzmann's thrombasthenia and treated for epist