Afibrinogenemia is a rare bleeding disorder with an estimated prevalence of 1:10,00,000 [1, 2]. It is an autosomal recessive disease resulting from mutations in any of the 3 genes that encodes the 3 polypeptide chains of fibrinogen and are located on the long arm of chromosome 4 3. Spontaneous bleeding, bleeding after minor trauma, and excessive bleeding during interventional procedures are the principal manifestations [2, 4]. Here we have reviewed the process of diagnosing a case of such rare disorder in Apollo Hospitals Dhaka. We have also highlighted the treatment and management plan of such a case.DOI: http://dx.doi.org/10.3329/pulse.v4i1.6964Pulse Vol.4 January 2010 p.34-35
| Mualliflar | Tahera Nazrin, Pinkoo Attawar, Md Moniruzzaman, I Islam |
|---|---|
| Jurnal | PULSE |
| Nashr sanasi | 2011-01-24 |
| Jild | 4 |
| Son | 1 |
| Betlar | 34-35 |
| Til | en |
| DOI | 10.3329/pulse.v4i1.6964 |
DOI: 10.3329/pulse.v4i1.6964 · Maqolaning asl sahifasi · PDF
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