Results 31 to 40 of about 1,146 (191)

Congenital Dysfibrinogenemia Presented with Massive Hematomas Formed after Hysterectomy [PDF]

, 2021
ArticleCase Reports in Clinical Medicine.
Niwa, Kentaro, Tanaka, Takuji, Niwa, Kenji, Nagata, Kentaro, Okumura, Nobuo, Nakagami, Takefumi, Takenaka, Motoki, Shimaoka, Ryuichiro   +7 more
core   +1 more source

Addressing some challenges of congenital fibrinogen disorders in 2023 and beyond

Bleeding, Thrombosis and Vascular Biology, 2023
Congenital fibrinogen disorders (CFD) include several types and subtypes of fibrinogen deficiency, resulting from monoallelic or biallelic mutations in one of the three fibrinogen genes. While it is relatively easy to make an accurate diagnosis based on
Cristina Santoro, Alessandro Casini
doaj   +3 more sources

Highly thrombogenic phenotype and impaired wound healing in a patient with congenital dysfibrinogenemia: case report. [PDF]

Res Pract Thromb Haemost
Background: Congenital fibrinogen disorders are classified based on both fibrinogen levels and the clinical phenotype. For dysfibrinogenemia, normal fibrinogen levels are typical.
El Beayni N, Szanto T, Neerman-Arbez M, Casini A, Lassila R.   +4 more
europepmc   +2 more sources

Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia. [PDF]

Blood Coagul Fibrinolysis
Rotational thromboelastometry (ROTEM) is a global hemostasis assay. The diagnosis added value of ROTEM in congenital dysfibrinogenemia remains to be established.
Simurda T, Marchi R, Casini A, Neerman-Arbez M, Drotarova M, Skornova I, Zolkova J, Kolkova Z, Loderer D, Brunclikova M, Belakova KM, Stasko J.   +11 more
europepmc   +2 more sources

Multiple Myeloma Presenting as Lower Gastrointestinal Bleeding: A Case Report. [PDF]

Clin Case Rep
ABSTRACT Multiple myeloma (MM) is a malignant hematologic neoplasm that primarily affects the bone marrow and can invade other organs, leading to diverse clinical manifestations. Presentation with gastrointestinal bleeding as the initial symptom is exceptionally rare.
Arabi A, Ambra N, Eltigani AMA, Yousif AA, Mohamed AH.   +4 more
europepmc   +2 more sources

Congenital dysfibrinogenemia as a rare cause of recurrent gastrointestinal bleeding [PDF]

, 2020
Introduction: Gastrointestinal bleeding is a common disease that surgeons encounter in everyday clinical practice. It is most often easy to diagnose and treat.
Lebowa, Weronika, Kenig, Jakub, Zdziarska, Joanna   +2 more
core   +1 more source

Dysfibrinogenemia

Blood & Vessel, 1971
openaire   +3 more sources

A 26-year-old pregnant woman with mild gingival bleeding

Clinical and Experimental Obstetrics & Gynecology, 2020
Congenital dysfibrinogenemia is a genetic coagulopathy that leads to compromised fibrinogen function. This case report describes a 26-year-old pregnant woman at the 38th week of gestation who presented with mild gingival bleeding and constant bruising on
J.Z. Zeng, Y. Dong, H.Y. Zhu, X. Xie, J.R. Liu, L. Li, Y.H. Zhai, Z. Cao   +7 more
doaj   +1 more source

Validating the Online Self-Administered Bleeding Assessment Tool (Self-BAT) as a Screening Tool for Bleeding Disorders. [PDF]

Haemophilia
Haemophilia, Volume 32, Issue 1, Page 324-327, January/February 2026.
DeYoung V, Grabell J, Hopman W, Chaigneau M, Avgeropoulos M, James P.   +5 more
europepmc   +2 more sources

Dysfibrinogenemia-Potential Impact of Genotype on Thrombosis or Bleeding

, 2022
The congenital dysfibrinogenemias, most often associated with bleeding disorders, encompass mutations in the amino-terminal end of fibrinogen α-chain consisting of Gly17-Pro18-Arg19-Val20, known as knob A, which is a critical site for fibrin ...
Feddersen, Søren, Kristensen, Søren Risom, Pedersen, Inge Søkilde; id_orcid, Pedersen, Inge Søkilde, Kristensen, Søren Risom; id_orcid, Sidelmann, Johannes Jakobsen, Bor, Mustafa Vakur, Feddersen, Søren; id_orcid   +7 more
core   +1 more source