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Management of an Infant with Hemophilia A
Pages 3-11
This clinical casebook provides a concise, state-of-the-art review of pediatric bleeding disorders. Presented in a case-based format, each case presents a different variant of bleeding disorder, illustrates the etiology, pathology, genetics, diagnosis, and management of the disorder, and offers clinical pearls. Disorders covered include hemophilia A and B, rare factor deficiencies, von Willebrand disease, immune thrombocytopenia purpura, and platelet dysfunctions.
Written by experts in the field, Pediatric Bleeding Disorders: A Clinical Casebook is a valuable resource for clinicians and practitioners treating patients with challenging coagulation issues.
Management of an Infant with Hemophilia A
Pages 3-11
Clinical Care of a Child with Hemophilia A and Inhibitors
Pages 13-23
Diagnosis and Management of a Patient with Newly Diagnosed Hemophilia B
Pages 25-33
Approach to a Child with Hemophilia B and Anaphylaxis to Factor IX
Pages 35-48
Manifestations and Treatment of Congenital Fibrinogen Deficiency
Pages 51-58
Diagnosis and Management of FVII Deficiency
Pages 59-64
Approach to Mucosal Bleeding in an Adolescent with FXI Deficiency
Pages 65-70
Recognition and Care of a Newborn with FXIII Deficiency
Pages 71-80
Classification and Management of Type 1 von Willebrand Disease
Pages 83-98
Presentation and Management of Type 2 von Willebrand Disease
Pages 99-112
Clinical Approach to Type 3 von Willebrand Disease
Pages 113-125
Pathophysiology and Management of Acquired von Willebrand Syndrome
Pages 127-137
Approach to a Patient with Sudden Onset of Mucocutaneous Bleeding and Thrombocytopenia
Pages 141-149
A Preteen Female with Fatigue and Incidental Finding of Thrombocytopenia
Pages 151-160
Diagnosis and Management of an Infant with Microthrombocytopenia
Pages 161-170
Care of a Toddler with Epistaxis and Bernard-Soulier Syndrome
Pages 171-182
Caring for an Infant with Heelstick Bleeding
Pages 185-194
Approach to a Child with Epistaxis and Macrothrombocytopenia
Pages 195-203
Recognition and Management of Congenital Platelet Granule Disorders
Pages 205-218
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