Factor XIII deficiency
Common Name(s)
Factor XIII deficiency
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Factor XIII deficiency" for support, advocacy or research.
To ensure that people affected by bleeding disorders have the freedom to make choices and seize opportunities To enable people affected by bleeding disorders to better understand and manage their condition or situation. To enable people affected by bleeding disorders to participate in decision making and service delivery. To influence policy and improve services to people with bleeding disorders.
How do you compare to others with this condition?
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Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Factor XIII deficiency" for support, advocacy or research.
To ensure that people affected by bleeding disorders have the freedom to make choices and seize opportunities To enable people affected by bleeding disorders to better understand and manage their condition or situation. To enable people affected by bleeding disorders to participate in decision making and service delivery. To influence policy and improve services to people with bleeding disorders.
http://www.haemophilia.org.uk/Recommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for Factor XIII deficiency can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
Scientific Literature
Articles from the PubMed Database
Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Factor XIII deficiency" returned 54 free, full-text research articles on human participants.
First 3 results:
Journal:
BACKGROUND Factor XIII deficiency is associated with recurrent miscarriages in women. CASE REPORT In this report, we present a patient with factor XIII deficiency and some comorbidities who had had previous miscarriages. She began treatment with factor XIII subunit A (XIII-A) replacement ...
Journal:
BACKGROUND Post-tonsillectomy hemorrhage (PTH) has been reported in the literature as a serious complication after tonsillectomy that has high morbidity and can be life threatening. In cases of recurrent secondary PTH, one should consider coagulopathies as the hidden pathology. Factor ...
Journal: Lab Med. 2016 Aug;47(3):220-6.
Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with an approximately 12-times higher than the rest of the world. The International Society for Thrombosis and Hemostasis (ISTH) suggested a standard algorithm for precise diagnosis and classification of FXIII deficiency ...
To view other free, full-text articles on human participants, please click on the link below.
Reviews from the PubMed Database
Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Factor XIII deficiency" returned 3 free, full-text review articles on human participants.
First 3 results:
Journal: Int J Lab Hematol. 2018 Feb;40(1):3-11.
Factor XIII deficiency (FXIIID) is a rare hereditary bleeding disorder arising from heterogeneous mutations, which can lead to life-threatening hemorrhage. The diagnosis of FXIIID is challenging due to normal standard coagulation assays requiring specific FXIII assays for diagnosis, ...
Journal: Dev Period Med. ;18(3):318-22.
Factor XIII (FXIII) deficiency is a rare, inherited or acquired coagulation disorder that potentially precipitates fatal haemorrhage. We report two consecutive pediatric patients with Henoch-Schönlein purpura (HSP) and symptomatic decrease in FXIII. The possible FXIII deficiency ...
To view other free, full-text review articles on human participants, please click on the link below.
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/gene/F13A1
https://ghr.nlm.nih.gov/gene/F13B
https://ghr.nlm.nih.gov/condition/factor-v-deficiency
https://ghr.nlm.nih.gov/condition/complement-factor-i-deficiency
https://ghr.nlm.nih.gov/condition/factor-x-deficiency
https://ghr.nlm.nih.gov/condition/factor-vii-deficiency
https://ghr.nlm.nih.gov/condition/factor-xi-deficiency
https://ghr.nlm.nih.gov/gene/COL13A1
https://ghr.nlm.nih.gov/condition/prothrombin-deficiency
https://ghr.nlm.nih.gov/condition/congenital-afibrinogenemia
https://ghr.nlm.nih.gov/gene/F10
https://ghr.nlm.nih.gov/condition/prekallikrein-deficiency
https://ghr.nlm.nih.gov/gene/F12
https://ghr.nlm.nih.gov/condition/factor-v-leiden-thrombophilia
https://ghr.nlm.nih.gov/gene/F5
https://ghr.nlm.nih.gov/condition/von-willebrand-disease
https://ghr.nlm.nih.gov/gene/CFI
https://ghr.nlm.nih.gov/gene/TNFRSF13B
https://ghr.nlm.nih.gov/gene/GFM1
There are currently no related results available in GeneReviews.
There are currently no related results available in Genetic Testing Registry.
Clinical Trial Information This information is provided by ClinicalTrials.gov
Condition Summary: Factor XIII Deficiency; ST-Elevation Myocardial Infarction; Myocardial Haemorrhage; Coronary Microvascular Disease
Condition Summary: Burns; Coagulation Disorder; Factor XIII Deficiency; Cicatrization; Endothelial Dysfunction
Condition Summary: Multiple Trauma; Coagulation Disorder; Coagulation Factor Deficiency; Coagulation Defect; Acquired
Finding the right clinical trial for Factor XIII deficiency can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.