2014
DOI: 10.1111/hae.12402
|View full text |Cite
|
Sign up to set email alerts
|

Rare bleeding disorders – bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency

Abstract: Rare bleeding disorders (RBDs) are inherited deficiencies of coagulation factors as fibrinogen, Factor (F) FII, FV, FVII, combined FV/FVIII, FX, FXI, and FXIII. These disorders have usually a low prevalence in the general population and constitute approximately 3 to 5% of all coagulation disorders. However, in some countries they could have the same prevalence of hemophilia B due to the practice of consanguineous marriage. The clinical picture of RBDs are highly variable and could markedly vary from mild to se… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4

Citation Types

3
78
0
7

Year Published

2016
2016
2022
2022

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 72 publications
(88 citation statements)
references
References 33 publications
3
78
0
7
Order By: Relevance
“…Hemostaz için gerekli minimum plazma faktör XI düzeyi 15-30 mg dL -1 olarak bildirilmektedir. Ancak, fazla replasman sonrasında tromboz gelişebilme riskine dikkat edilmelidir (6). Konsantre faktör XI hazırlan-ması zor ve pahalıdır.…”
Section: Olgu Sunumuunclassified
See 3 more Smart Citations
“…Hemostaz için gerekli minimum plazma faktör XI düzeyi 15-30 mg dL -1 olarak bildirilmektedir. Ancak, fazla replasman sonrasında tromboz gelişebilme riskine dikkat edilmelidir (6). Konsantre faktör XI hazırlan-ması zor ve pahalıdır.…”
Section: Olgu Sunumuunclassified
“…Gerekli replasman miktarının hesaplanmasında yapılacak Turk J Anaesthesiol Reanim 2016; 44: 149-51 cerrahinin büyüklüğü, kanama potansiyeli, hastanın faktör düzeyi önemlidir. (3,6). Bizim hastamızda preoperatif 20 mL kg -1 ve intraoperatif 10 mL kg -1 olacak şekilde TDP verildi.…”
Section: Olgu Sunumuunclassified
See 2 more Smart Citations
“…VIII, VII, X, XI, and XIII. 2,3 Their prevalence is very low, ranging from 1:500,000 for FVII deficiency to 1:2,000,000 for prothrombin and FXIII deficiency. 2 Inherited platelet function disorders are much more common.…”
mentioning
confidence: 99%