Semin Thromb Hemost 2011; 37(7): 737-744
DOI: 10.1055/s-0031-1297164
© Thieme Medical Publishers

Pediatric Hemophilia: A Review

Roshni Kulkarni1 , J. Michael Soucie2
  • 1Department of Pediatrics and Human Development, Michigan State University, East Lansing, Michigan
  • 2Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia
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Publikationsverlauf

Publikationsdatum:
20. Dezember 2011 (online)

ABSTRACT

The hemophilias are the most common X-linked inherited bleeding disorders, which if not properly managed can lead to chronic disease and lifelong disabilities. The challenges and issues in newborns are different from that in older children and adults. Bleeding events still predominate as the diagnostic trigger in children, however, the sites of bleeding vary with age. While delivery-associated intracranial hemorrhage (ICH), circumcision, and venipuncture bleeding are common in the newborn period, joint disease and head trauma occur in the older child and adolescent. Awareness of clinical manifestations and treatment complications are crucial in instituting appropriate management and implementing preventive strategies. Currently, inhibitors and ICH are the most challenging complications and prophylaxis is emerging as the optimal preventive care strategy.

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Roshni KulkarniM.D. 

Professor and Director, Pediatric & Adolescent Hematology/Oncology; Director (Pediatrics), MSU Centers for Bleeding and Clotting Disorders; Former Director and Distinguished Hematology Consultant, Division of Blood Disorders

CDC, B 216 Clinical Center; Department of Pediatrics and Human Development, Michigan State University, East Lansing, MI 48824

eMail: Roshni.Kulkarni@hc.msu.edu

eMail: Roshni@msu.edu