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Congenital Bleeding Disorders: Diagnosis and Management
 
Product details:
ISBN13:9783031431555
ISBN10:3031431553
Binding:Hardback
No. of pages:463 pages
Size:235x155 mm
Weight:1010 g
Language:English
Illustrations: 7 Illustrations, black & white; 95 Illustrations, color
666
Category:

Congenital Bleeding Disorders

Diagnosis and Management
 
Edition number: 2nd ed. 2023
Publisher: Springer
Date of Publication:
Number of Volumes: 1 pieces, Book
 
Normal price:
Publisher's listprice:
EUR 213.99
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88 302 HUF (84 098 HUF + 5% VAT)
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70 642 (67 278 HUF + 5% VAT )
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Estimated delivery time: In stock at the publisher, but not at Prospero's office. Delivery time approx. 3-5 weeks.
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Short description:

This significantly updated new edition describes in detail the clinical presentations, diagnosis, and management of a wide range of congenital bleeding disorders. It will assist readers in overcoming the significant challenges involved in clinical and laboratory diagnosis and in providing effective clinical care that makes optimal use of new products, including recombinant factor concentrate. The coverage ranges from hemophilia A and B and von Willebrand disease to rare bleeding disorders such as congenital factor V, factor X, factor XI, and factor XIII deficiency and inherited platelet function disorders. The exceptional attention to rarer conditions is of particular importance given the considerable risk of overlooking them during diagnosis, with potential consequences for disease-related morbidity and mortality. The authors are acknowledged specialists in the field from across the world who have particular expertise in the disorder that they discuss. The book will be of value tohematologists, oncologists, pediatricians, laboratory specialists and technicians, general physicians, and trainees.

Long description:
This significantly updated new edition describes in detail the clinical presentations, diagnosis, and management of a wide range of congenital bleeding disorders. It will assist readers in overcoming the significant challenges involved in clinical and laboratory diagnosis and in providing effective clinical care that makes optimal use of new products, including recombinant factor concentrate. The coverage ranges from hemophilia A and B and von Willebrand disease to rare bleeding disorders such as congenital factor V, factor X, factor XI, and factor XIII deficiency and inherited platelet function disorders. The exceptional attention to rarer conditions is of particular importance given the considerable risk of overlooking them during diagnosis, with potential consequences for disease-related morbidity and mortality. The authors are acknowledged specialists in the field from across the world who have particular expertise in the disorder that they discuss. The book will be of value to hematologists, oncologists, pediatricians, laboratory specialists and technicians, general physicians, and trainees.

Table of Contents:

 An Overview of Hemostasis.- Congenital Bleeding Disorders: Diagnosis and Management.- von Willebrand disease: an update on diagnosis and treatment.- Hemophilia A, Diagnosis and Management.- Hemophilia B, Diagnosis and Management.- Congenital fibrinogen disorders, diagnosis, and management.- Congenital Prothrombin Deficiency: Diagnosis and Management.- Congenital Factor V Deficiency.- Combined Factor V and Factor VIII Deficiency, Diagnosis and Management.- Congenital Factor VII Deficiency, Diagnosis and Management.- Vitamin K-dependent Coagulation Factors Deficiency, Diagnosis and Management.- Congenital Factor X deficiency, Diagnosis and Management.- Congenital Factor XI Deficiency.- Congenital Factor XIII Deficiency, Diagnosis and Management.- Glanzmann Thrombasthenia.- Bernard-Soulier Syndrome, Diagnosis and Management.- Gray Platelet Syndrome (GPS).