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Pediatric Radiology

, Volume 30, Issue 6, pp 420–423 | Cite as

Inherited protein-C deficiency, factor V G 1691 A and FV A 4070 G mutations in a child with internal cerebral venous thrombosis

  • T. Sipahi
  • Ç. Üner
  • Y. T. Yıldız
  • N. Akar
Original article

Abstract

Common systemic disorders that cause cerebral venous thrombosis (CVT) in children include dehydration, trauma, infection and haematological diseases. No cause for CVT is identified in one quarter of all cases. We report a child with thalamic infarcts due to internal CVT who had congenital heterozygous protein-C deficiency, factor V G 1691 A and A 4070 G mutations.

Keywords

Dehydration Venous Thrombosis Factor Versus Systemic Disorder Haematological Disease 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2000

Authors and Affiliations

  • T. Sipahi
    • 1
  • Ç. Üner
    • 2
  • Y. T. Yıldız
    • 2
  • N. Akar
    • 3
  1. 1.Department of Paediatric Haematology, Dr Sami Ulus Children's Medical Centre, Altındağ, Ankara, TurkeyTR
  2. 2.Department of Paediatric Radiology, Dr Sami Ulus Children's Medical Centre, Altındağ, Ankara, TurkeyTR
  3. 3.Department of Molecular Pathology, Ankara University, Ankara, TurkeyTR

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