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A novel frameshift mutation in FGA (c. 1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family

E Levrat, I Aboukhamis, P de Moerloose… - Blood Coagulation & …, 2011 - journals.lww.com
... Case Reports. A novel frameshift mutation in FGA (c.1846 del A) leading to congenital
afibrinogenemia in a consanguineous Syrian family. ... Most reported mutations leading to
congenital afibrinogenemia are located in FGA encoding the fibrinogen A α-chain. ...
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Successive bleeding and thrombotic complications in a patient with afibrinogenemia: A case report.

Y Chevalier, Y Dargaud, L Argaud, J Ninet… - Thrombosis …, 2011 - ncbi.nlm.nih.gov
... 2011 Apr 13. [Epub ahead of print] Successive bleeding and thrombotic complications in a patient
with afibrinogenemia: A case report. Chevalier Y, Dargaud Y, Argaud L, Ninet J, Jouanneau E,
Négrier C. Unité d'Hémostase Clinique, Hopital Edouard Herriot, Lyon, France. ...
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[HTML] Cellulitis on face in a patient with congenital afibrinogenemia

[HTML] from jisppd.comGD Chandan, AG Annaji, S Bhatnagar… - Journal of Indian …, 2011 - Medknow
... Cellulitis on face in a patient with congenital afibrinogenemia GD Chandan 1 , AG Annaji 2 , S
Bhatnagar 3 , U Mohandas 1 , P Dave 1 1 Department of Pedodontics and Preventive Dentistry,
VS Dental College and Hospital, Bangalore, India 2 Department of Oral Medicine and ...
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[PDF] Afibrinogenemia

[PDF] from banglajol.infoT Nazrin, P Attawar, M Moniruzzaman… - Pulse, 2011 - banglajol.info
Page 1. Afibrinogenemia 1 2 3 4 ... Abstract 1,2 Afibrinogenemia is a rare bleeding disorder with
an estimated prevalence of 1: 10,00,000. It is an autosomal recessive disease resulting from
mutations in any of the 3 genes that encodes the 3 polypeptide chains of fibrinogen 3 ...
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Spontaneous Bilateral Subhyaloid Hemorrhage in Congenital Hypofibrinogenemia

A Pathengay, S Ambatipudi… - Retinal Cases and Brief …, 2011 - journals.lww.com
... Congenital afibrinogenemia and hypofibrinogenemia are rare disorders. Unlike congenital ...
affected families. Congenital hypofibrinogenemia occurs commonly in the heterozygous
genotype and afibrinogenemia in the homozygous genotype. ...
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