Results 1 to 10 of about 448,079 (362)

Case Report: Factor VII Deficiency Presented With Cephalohematoma After Birth [PDF]

Frontiers in Pediatrics, 2021
Introduction: Factor VII deficiency is a rare inherited autosomal recessive bleeding disorder with a global prevalence of 1/500,000. Most cases remain asymptomatic, and cases with severe clinical presentation are rarely reported.Case Presentation: A ...
Yuan-Chun Lo, Ching-Tien Peng, Ching-Tien Peng, Yin-Ting Chen   +3 more
doaj   +3 more sources

Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency. [PDF]

J Clin Lab Anal, 2021
Hereditary human coagulation factor VII (FVII) deficiency is an inherited autosomal recessive hemorrhagic disease involving mutations in the F7 gene. The sites and types of F7 mutations may influence the coagulation activities of plasma FVII (FVII: C ...
Zhang X, Wang S, Leng S, Feng Q, Zhang Y, Xu S, Zhang L, Zhang X, Fang Y, Peng J, Sheng Z.   +10 more
europepmc   +4 more sources

Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER)

Haematologica, 2013
Because of the very short half-life of factor VII, prophylaxis in factor VII deficiency is considered a difficult endeavor. The clinical efficacy and safety of prophylactic regimens, and indications for their use, were evaluated in factor VII-deficient ...
Mariasanta Napolitano, Muriel Giansily-Blaizot, Alberto Dolce, Jean F. Schved, Guenter Auerswald, Jørgen Ingerslev, Jens Bjerre, Carmen Altisent, Pimlak Charoenkwan, Lisa Michaels, Ampaiwan Chuansumrit, Giovanni Di Minno, Ümran Caliskan, Guglielmo Mariani   +13 more
doaj   +4 more sources

Reproductive health and hemostatic issues in women and girls with congenital factor VII deficiency: A systematic review. [PDF]

J Thromb Haemost, 2022
Congenital factor VII (FVII) deficiency is an inherited bleeding disorder, with heterogenous bleeding symptoms. Women with FVII deficiency face hemostatic challenges during menstruation, ovulation, and childbirth.
Abdul-Kadir R, Gomez K.
europepmc   +2 more sources

Mutations of TFPI-binding exosites on factor VII cause bleeding phenotypes in factor VII deficiency. [PDF]

Blood Adv, 2022
Key Points • TFPI-binding exosite mutations have been reported in patients with FVII deficiency and clinical bleeding variabilities.• The alteration of TFPI-binding exosites of FVII affected FVII secretion and the binding with FX, resulting in abnormal ...
Seanoon K, Payongsri P, Vivithanaporn P, Sirachainan N, Chuansumrit A, Hongeng S, Tanratana P.   +6 more
europepmc   +2 more sources

Diagnosis and treatment discussion of congenital factor VII deficiency in pregnancy: A case report. [PDF]

World J Clin Cases, 2021
BACKGROUND Congenital factor VII deficiency (FVIID) is a rare autosomal recessive genetic disorder. The clinical manifestations of this deficiency vary greatly. Predicting the risk of bleeding during and after childbirth of pregnant women with congenital
Yang Y, Zeng YC, Rumende P, Wang CG, Chen Y.   +4 more
europepmc   +2 more sources

Inhibitor in Congenital Factor VII Deficiency; a Rare but Serious Therapeutic Challenge-A Systematic Literature Review. [PDF]

J Clin Med, 2021
Background: Congenital factor (F) VII deficiency is a rare coagulation factor deficiency with an estimated incidence of 1 per 500,000 individuals. Patients with severe FVII deficiency present a broad range of clinical presentations.
Ramezanpour N, Zaker F, Biswas A, Dorgalaleh A.   +3 more
europepmc   +2 more sources

Acute Myelogenous Leukemia With Trisomy 8 and Concomitant Acquired Factor VII Deficiency

Journal of Investigative Medicine High Impact Case Reports, 2019
Acquired isolated factor VII deficiency is a rare bleeding disorder and has been reported in 31 cases. This is in contrast to congenital factor VII deficiency, which while also infrequent is the most common rare congenital bleeding disorder.
Leila Moosavi MD, Jonathan Bowen BSc, Jeffrey Coleman MD, Arash Heidari MD, Everardo Cobos MD   +4 more
doaj   +2 more sources

Use of recombinant factor VIIa for hip surgery in a patient with factor-VII deficiency: A case report [PDF]

, 2007
patient with factor-VII deficiency: A case ...
Cashen, Amanda F., Clohisy, John C., Eby, Charles S., Gopalan, Priya K.   +3 more
core   +4 more sources

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies [PDF]

Haemophilia, 2016
A paucity of data exists on the incidence, diagnosis and treatment of bleeding in women with inherited factor VII (FVII ...
Batorova, Baumann Kreuziger, Bernardi, Byams, Di Minno, Fasouliotis, Foster, Grant, James, James, Kadir, Kadir, Kadir, Kirtava, Kitchens, Kouides, Kouides, Kulkarni, Kulkarni, Lobo, Lobo, Mariani, Mariani, Mariani, Mariani, Mariani, Napolitano, Napolitano, Peyvandi, Shankar, Warner, Warner, Wellington   +32 more
core   +3 more sources