Congenital afibrinogenemia in a newborn

Autor: Özay Mustafa, Kara Mustafa, Keskin Zuhal

Publikováno v: Sanamed, Vol 17, Iss 3, Pp 185-188 (2022)

Introduction: Congenital afibrinogenemia is a rare coagulation disorder characterized by a deficiency in the fibrinogen molecule. Fibrinogen is a hexameric glycoprotein consisting of a polypeptide chain encoded by FGB, FGA, and FGG and is required fo

Externí odkaz: https://doaj.org/article/d0a9638a569e4019ae4d5613eb920990

Endovascular Treatment for Lower-extremity Arterial Thrombosis in a Patient with Congenital Afibrinogenemia and a History of Bleeding Complications

Autor: Tairo Kurita, Akihiro Takasaki, Takeshi Matsumoto, Ryuji Okamoto, Yoshito Ogihara, Kei Sato, Hideo Wada, Daisuke Hiramatsu, Kaoru Dohi

Publikováno v: Internal Medicine. 61:361-364

Congenital afibrinogenemia is a rare autosomal recessive blood disorder that accompanies thrombotic complications and is associated with bleeding tendency. The management of these opposing complications remains a challenge. Endovascular treatment (EV

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b39902c378ddf13e9b0d1a0b3ee1b8e5
https://doi.org/10.2169/internalmedicine.7542-21

Identification of a novel mutation in congenital afibrinogenemia in Iranian patients

Autor: Somayeh Takrim Nojehdeh, Mahboobeh Masoodifard, Sirous Zeinali, Marzieh Mojbafan, Masoume Amini

Publikováno v: Blood Coagulation & Fibrinolysis. 32:323-327

Congenital afibrinogenemia is a rare autosomal recessive disorder that is caused by defects in the fibrinogen. Fibrinogen is a hexameric glycoprotein made of two pairs of three homologous polypeptide chains including Aα, Bβ, and γ that are encoded

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cdccb6672d05c4f60ce97f9201059a8
https://doi.org/10.1097/mbc.0000000000001041

Agudização da afibrinogenemia congênita: um relato de caso / Acute worsening of congenital afibrinogenemia: a case report

Autor: Yasmin Melo Toledo, Michelle Rafaelle Andrade Gurgel, Maria Eduarda Butarelli Nascimento, Ilca Pereira Prado, Lunna Oliveira Santos, Yasmin Oliveira Santos

Publikováno v: Brazilian Journal of Health Review; Vol. 4 No. 1 (2021); 3652-3655
Brazilian Journal of Health Review; v. 4 n. 1 (2021); 3652-3655
Brazilian Journal of Health Review
Federação das Indústrias do Estado do Paraná (FIEP)
instacron:BJRH

INTRODUÇÃO: A afibrinogenemia congênita, também conhecida como síndrome do fibrinogênio circulante indetectável, é um distúrbio autossômico recessivo extremamente raro, estimado em um a cada um milhão de habitantes. É uma alteração advi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af244b613708315dbdf854655e7a0430
https://doi.org/10.34119/bjhrv4n1-287

Liver transplantation as a novel strategy for resolution of congenital afibrinogenemia in a pediatric patient

Autor: Guillermo De Angulo, Tamir Miloh, Akin Tekin, Fernando F. Corrales-Medina, David M. Andrews, Candelaria O’Farrell

Publikováno v: Journal of Thrombosis and Haemostasis

Fibrinogen replacement therapy is a treatment mainstay for patients with afibrinogenemia and significant bleeding. A male infant with congenital afibrinogenemia and several spontaneous hemarthroses commenced cryoprecipitate prophylaxis but developed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a98999852409977ac5dc489dea0ffc63
http://europepmc.org/articles/PMC7756576