Afibrinogenemia

Tahera Nazrin, Pinkoo Attawar, Md Moniruzzaman, I Islam

PULSE · 2011-yil

Annotatsiya

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

Maqola ma’lumotlari
MualliflarTahera Nazrin, Pinkoo Attawar, Md Moniruzzaman, I Islam
JurnalPULSE
Nashr sanasi2011-01-24
Jild4
Son1
Betlar34-35
Tilen
DOI10.3329/pulse.v4i1.6964

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