Haemophilia patient had variant CJD agent in spleen

BMJ 2009; 338 doi: 10.1136/bmj.b705 (Published 18 February 2009)
Cite this as: BMJ 2009;338:b705

Access to the full text of this article requires a subscription or payment. Please log in or subscribe below.

  1. Lynn Eaton
  1. 1London

    A postmortem of a 70 year old patient with haemophilia has shown that he had the abnormal prion protein for Creutzfeldt-Jakob Disease (vCJD) in his spleen. It is the first time the vCJD agent has been found in a patient with haemophilia or anyone treated with a plasma product.

    The patient’s death was unrelated to vCJD, and he had no symptoms of the disease or any other neurological condition before his death. However, the …

    Access to the full text of this article requires a subscription or payment

    Article access

    Article access for 1 day

    Purchase this article for £20 $30 €32*

    The PDF version can be downloaded as your personal record

    * Prices do not include VAT

    THIS WEEK'S POLL