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Congenital bleeding disordersdiagnos...

Dorgalaleh, Akbar.

Congenital bleeding disordersdiagnosis and management /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Congenital bleeding disordersedited by Akbar Dorgalaleh.
Reminder of title:	diagnosis and management /
other author:	Dorgalaleh, Akbar.
Published:	Cham :Springer International Publishing :2018.
Description:	xiv, 396 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
Subject:	BloodDiseases.
Online resource:	http://dx.doi.org/10.1007/978-3-319-76723-9
ISBN:	9783319767239$q(electronic bk.)

Congenital bleeding disordersdiagnosis and management /
Congenital bleeding disordersdiagnosis and management /[electronic resource] :edited by Akbar Dorgalaleh. - Cham :Springer International Publishing :2018. - xiv, 396 p. :ill., digital ;24 cm.

Part I: Common bleeding disorders -- 1. Von Willebrand disease -- 2. Hemophilia A (congenital factor VIII deficiency) -- 3. Hemophilia B (congenital factor IX deficiency) Part II: Rare bleeding disorders -- 4. Congenital factor I (fibrinogen) disorders -- 5. Congenital factor II deficiency -- 6. Congenital factor V deficiency -- 7. Combined coagulation factor deficiencies -- 8. Congenital factor VII deficiency -- 9. Congenital factor X deficiency -- 10. Congenital factor XI deficiency -- 11. Congenital factor XIII deficiency Part III: Inherited platelet function disorders -- 12. Glanzmann thrombasthenia -- 13. Bernard-Soulier syndrome -- 14. Gray platelet syndrome -- 15. Quebec platelet disorder.

This book describes in detail the clinical presentation, 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.

ISBN: 9783319767239$q(electronic bk.)

Standard No.: 10.1007/978-3-319-76723-9doiSubjects--Topical Terms:

318459
Blood
--Diseases.

LC Class. No.: RC633 / .C664 2018

Dewey Class. No.: 616.15

Congenital bleeding disordersdiagnosis and management /
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505 0 $a Part I: Common bleeding disorders -- 1. Von Willebrand disease -- 2. Hemophilia A (congenital factor VIII deficiency) -- 3. Hemophilia B (congenital factor IX deficiency) Part II: Rare bleeding disorders -- 4. Congenital factor I (fibrinogen) disorders -- 5. Congenital factor II deficiency -- 6. Congenital factor V deficiency -- 7. Combined coagulation factor deficiencies -- 8. Congenital factor VII deficiency -- 9. Congenital factor X deficiency -- 10. Congenital factor XI deficiency -- 11. Congenital factor XIII deficiency Part III: Inherited platelet function disorders -- 12. Glanzmann thrombasthenia -- 13. Bernard-Soulier syndrome -- 14. Gray platelet syndrome -- 15. Quebec platelet disorder.
520 $a This book describes in detail the clinical presentation, 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.
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