Congenital Bleeding Disorders -

Congenital Bleeding Disorders

Diagnosis and Management

Akbar Dorgalaleh (Herausgeber)

Buch | Hardcover
XIV, 396 Seiten
2018 | 1st ed. 2018
Springer International Publishing (Verlag)
978-3-319-76722-2 (ISBN)
149,79 inkl. MwSt
zur Neuauflage
  • Titel erscheint in neuer Auflage
  • Artikel merken
Zu diesem Artikel existiert eine Nachauflage
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. 

Akbar Dorgalaleh, hematologist and scientific researcher in the field of congenital bleeding disorders in the Department of Hematology and Blood Transfusion, Iran University of Medical Sciences (IUMS). Dr. Dorgalaleh's primary interest is the diagnosis and management of congenital bleeding disorders, and he has a special interest in congenital factor XIII deficiency. He acts as a reviewer for several international journals in the field of Hematology and to date has authored about 100 papers that cover all the congenital bleeding disorders, including hemophilia, rare bleeding disorders, and inherited platelet function disorders. He has reported the clinical, laboratory, and molecular characteristics of a very large number of patients with congenital bleeding disorders.

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.

 

 

Erscheinungsdatum
Zusatzinfo XIV, 396 p. 93 illus., 85 illus. in color.
Verlagsort Cham
Sprache englisch
Maße 155 x 235 mm
Gewicht 697 g
Themenwelt Medizinische Fachgebiete Innere Medizin Hämatologie
Medizin / Pharmazie Medizinische Fachgebiete Pädiatrie
Schlagworte Bernard-Soulier Syndrome • Combined Coagulation Factor Defiencies • Common Bleeding Disorders • Congenital Factor I disorders • Congenital Factor II deficiency • Congenital Factor V deficiency • Congenital Factor VII deficiency • Congenital Factor X deficiency • Glanzmann Thrombasthenia • Gray Platelet Syndrome • Hemophilia A • Hemophilia B • Quebec Platelet Disorder • Rare Bleeding Disorders • Von Willebrand Disorders
ISBN-10 3-319-76722-4 / 3319767224
ISBN-13 978-3-319-76722-2 / 9783319767222
Zustand Neuware
Haben Sie eine Frage zum Produkt?
Wie bewerten Sie den Artikel?
Bitte geben Sie Ihre Bewertung ein:
Bitte geben Sie Daten ein:
Mehr entdecken
aus dem Bereich
Hämatologie und Internistische Onkologie

von Dietmar P. Berger; Monika Engelhardt; Justus Duyster

Buch | Softcover (2023)
ecomed-Storck GmbH (Verlag)
129,99