Literature DB >> 7885016

[Case report of congenital afibrinogenemia].

J V Leeners1, J Mossakowski, S Kayser.   

Abstract

It is reported about a case of congenital afirinogenaemia on a newborn female. The treatment is described. Congenital afirinogenaemia is a rare autosomal recessive disorder. There are 250 cases in world literature, mostly with consanguineous parents. Bleeding is usually mild, so that treatment should not be prophylactic, because any blood product might cause complication, like AIDS. Only acute haemorrhage should be treated with fresh frozen plasma or fibrinogen concentrates.

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Year:  1995        PMID: 7885016     DOI: 10.1055/s-2008-1046506

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  2 in total

1.  Congenital Afibrinogenemia presenting as antenatal intracranial bleed: a case report.

Authors:  Gopakumar Hariharan; Sivji Ramachandran; Rajiv Parapurath
Journal:  Ital J Pediatr       Date:  2010-01-05       Impact factor: 2.638

2.  Hemophilia A and congenital hypofibrinogenemia: a rare association in same family.

Authors:  Biswanath Basu
Journal:  Indian J Pediatr       Date:  2010-02       Impact factor: 1.967

  2 in total

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