Haemophilia B
From Wikipedia, the free encyclopedia
| ICD-10 | D67. |
|---|---|
| ICD-9 | 286.1 |
| OMIM | 306900 |
| DiseasesDB | 5561 |
| MedlinePlus | 000539 |
| eMedicine | emerg/240 |
Haemophilia B (also spelled Hemophilia B or Hæmophilia B) is a blood clotting disorder caused by a mutation of the Factor IX gene. It is the second most common form of haemophilia, rarer than haemophilia A. It is sometimes called Christmas disease after Stephen Christmas, the first patient described with this disease. In addition, the first report of its identification was published in the Christmas edition of the British Medical Journal.
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[edit] Treatment
Treatment (bleeding prophylaxis) is by intravenous infusion of factor IX.
[edit] Genetics
The factor IX gene is located on the X chromosome (Xq27.1-q27.2). It is inherited X-linked recessive, which explains why - as in haemophilia A - only males are generally affected.
[edit] Pathophysiology
Factor IX deficiency leads to an increased propensity for haemorrhage. This is in response to mild trauma or even spontaneously, such as in joints (haemarthrosis) or muscles.
[edit] Reference
- Biggs RA, Douglas AS, MacFarlane RG, Dacie JV, Pittney WR, Merskey C, O'Brien JR. Christmas disease: a condition previously mistaken for haemophilia. Br Med J 1952;2:1378-1382. PMID 12997790.
[edit] External links
- Your genes your health page on Haemophilia B.
- synd/2321 at Who Named It
- GPnotebook -1529872380
- FPnotebook HEM17
