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| Content Provider | PubMed Central |
|---|---|
| Author | Dukka, Srivasavi Allsup, David John |
| Copyright Year | 2013 |
| Abstract | Type 2N Von Willebrand's disease (2N VWD) is a rare, recessively inherited bleeding disorder, comprising 1-2% of all VWD patients, usually manifesting as a mild bleeding diathesis. Treatment includes desmopressin (DDAVP) or intermediate purity plasma-derived FVIII concentrates containing residual VWF. We present a case of a 75-year-old gentleman, incidentallydiagnosed with type 2N VWD in 2002 on routine blood testing before surgery with an ISTH bleeding score of 1-2, who was treated with recombinant FVIII preoperatively. |
| Related Links | http://dx.doi.org/10.1155/2013/837906 |
| Starting Page | 837906 |
| File Format | |
| ISSN | 20906560 |
| e-ISSN | 20906579 |
| Journal | Case Reports in Hematology |
| Volume Number | 2013 |
| Language | English |
| Publisher | Hindawi Publishing Corporation |
| Publisher Date | 2013-01-01 |
| Access Restriction | Open |
| Rights Holder | Hindawi Publishing Corporation |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
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