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Congenital bleeding disorders = diagnosis and management /

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Congenital bleeding disorders/ edited by Akbar Dorgalaleh.
Reminder of title:	diagnosis and management /
other author:	Dorgalaleh, Akbar.
Published:	Cham :Springer International Publishing : : 2023.,
Description:	xvi, 463 p. :ill. (some col.), digital ; : 24 cm.;
Contained By:	Springer Nature eBook
Subject:	Blood coagulation disorders. -
Online resource:	https://doi.org/10.1007/978-3-031-43156-2
ISBN:	9783031431562

Congenital bleeding disorders = diagnosis and management /
Congenital bleeding disordersdiagnosis and management /[electronic resource] :edited by Akbar Dorgalaleh. - Second edition. - Cham :Springer International Publishing :2023. - xvi, 463 p. :ill. (some col.), digital ;24 cm.

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)

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.

ISBN: 9783031431562

Standard No.: 10.1007/978-3-031-43156-2doiSubjects--Topical Terms:

645020
Blood coagulation disorders.

LC Class. No.: RC647.C55

Dewey Class. No.: 616.15

Congenital bleeding disorders = diagnosis and management /
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505 0 $a 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)
520 $a 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.
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