Congenital factor XIII deficiency with multiple connective tissue tumours and successful pregnancy with substitutive therapy (a case report)

1992 ◽  
Vol 3 (6) ◽  
pp. 810
Author(s):  
Z. Boda ◽  
G. Pfliegler ◽  
L. Muszbek ◽  
A. T??th ◽  
R. ??d??ny ◽  
...  
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Factor Xiii ◽  
Factor Xiii Deficiency ◽  
Successful Pregnancy ◽  
Congenital Factor

Successful pregnancy in a woman with congenital factor XIII deficiency treated with substitutive therapy

1987 ◽  
Vol 55 (1) ◽  
pp. 45-48 ◽  
Author(s):  
F. Rodeghiero ◽  
G. C. Castaman ◽  
E. Bona ◽  
M. Ruggeri ◽  
E. Dini
Keyword(s):  
Factor Xiii ◽  
Factor Xiii Deficiency ◽  
Successful Pregnancy ◽  
Congenital Factor

Congenital factor XIII deficiency with the presence of inhibitor: a case report

2019 ◽  
Vol 85 ◽  
pp. S82-S83
Author(s):  
S. Karaman ◽  
A. Unuvar ◽  
D. Tugcu ◽  
F. Bilgili ◽  
S. Genc ◽  
...  
Keyword(s):  
Case Report ◽  
Factor Xiii ◽  
Factor Xiii Deficiency ◽  
Congenital Factor

Congenital Factor XIII Deficiency with Multiple Benign Breast Tumours and Successful Pregnancy with Substitutive Therapy

1989 ◽  
Vol 19 (6) ◽  
pp. 348-352 ◽  
Author(s):  
Z. Boda ◽  
G. Pfliegler ◽  
L. Muszbek ◽  
A. Tóth ◽  
R. Ádány ◽  
...  
Keyword(s):  
Factor Xiii ◽  
Factor Xiii Deficiency ◽  
Successful Pregnancy ◽  
Breast Tumours ◽  
Congenital Factor

scholarly journals A CASE REPORT WITH SEVERE CONGENITAL FACTOR XIII DEFICIENCY AND AN UNCOMPLICATED PREGNANCY AND BIRTH PROCESS

2021 ◽  
Vol 43 ◽  
pp. S53-S54
Author(s):  
İbrahim Eker ◽  
Yeter Düzenli Kar ◽  
Nilgün Eroğlu ◽  
Özge Vural ◽  
Mehmet Yılmazer
Keyword(s):  
Case Report ◽  
Factor Xiii ◽  
Birth Process ◽  
Factor Xiii Deficiency ◽  
Uncomplicated Pregnancy ◽  
Pregnancy And Birth ◽  
Congenital Factor

New Families with Hereditary Hemorrhagic Trait due to Deficiency of Fibrin Stabilizing Factor (F. XIII)

1968 ◽  
Vol 20 (03/04) ◽  
pp. 534-541 ◽  
Author(s):  
O Egeberg
Keyword(s):  
Factor Xiii ◽  
Family Members ◽  
Recessive Inheritance ◽  
Factor Xiii Deficiency ◽  
History Of ◽  
Congenital Factor

SummarySevere hemorrhagic disorder due to congenital factor XIII deficiency is described in two unrelated Norwegian girls.Plasma cephalin time was for both patients extraordinarily short during episodes of bleeding and hematomas. No such hyperactivity reaction was demonstrable in unaffected condition some months later.Estimations of blood factor XIII levels revealed a partial defect in the parents of both children, and also in some other family members, consistent with an autosomal incompletely recessive inheritance of the defect. Some of the presumptive heterozygotes had a history of light bleeding phenomenons; whether this was related to their partial lack of factor XIII is so far uncertain.

scholarly journals A Novel Molecular Mechanism of Severe Congenital Factor XIII Deficiency

2020 ◽  
Author(s):  
Jingjing Han ◽  
Miao Jiang ◽  
Jian Su ◽  
Ziqiang Yu ◽  
Xia Bai ◽  
...  
Keyword(s):  
Molecular Mechanism ◽  
Factor Xiii ◽  
Factor Xiii Deficiency ◽  
Congenital Factor

Noninvasive prenatal diagnosis of congenital factor XIII deficiency in Iran

2022 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Hoda Motlagh ◽  
Akbar Dorgalaleh ◽  
Shadi Tabibian ◽  
Majid Naderi ◽  
Farhad Zaker
Keyword(s):  
Prenatal Diagnosis ◽  
Factor Xiii ◽  
Factor Xiii Deficiency ◽  
Noninvasive Prenatal Diagnosis ◽  
Congenital Factor

scholarly journals Use of Catridecacog in a patient with severe Factor XIII deficiency undergoing surgery

2019 ◽  
Vol 11 (1) ◽  
Author(s):  
Gianluca Sottilotta ◽  
Francesca Luise ◽  
Vincenzo Oriana ◽  
Angela Piromalli ◽  
Rosa Santacroce ◽  
...  
Keyword(s):  
Inguinal Hernia ◽  
Surgical Procedures ◽  
Factor Xiii ◽  
Bleeding Disorder ◽  
Factor Xiii Deficiency ◽  
Fxiii Deficiency ◽  
Congenital Factor

Despite many articles regarding the antihemorrhagic treatment and prophylaxis, there is a lack of experience about how to best conduct major surgical procedures in patients with congenital factor XIII (FXIII) deficiency. Here we report a case of surgery (right inguinal hernia, complicated by heaviness and pain) performed in a patient with FXIII deficiency, receiving recombinant FXIII prophylaxis (Catridecacog 35 UI/kg every 28±2 days). Our experience shows that Catridecacog can be used safely and effectively not only for continued prophylaxis but also in surgery and adds to the very limited body of evidence currently available on surgery in this bleeding disorder.

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