Results 51 to 60 of about 448,079 (362)

Impact of Rare Bleeding Disorders during Pregnancy on Maternal and Fetal Outcomes: Review of 29 Pregnancies at a Single Center [PDF]

Revista Brasileira de Ginecologia e Obstetrícia, 2017
Objective: This study aims to give information about the relationship between different types of factor deficiencies and maternal/obstetric outcomes. Methods We retrospectively reviewed the medical records of eight women with factor deficiency disorders.
Gokcen Orgul, Fatih Aktoz, M. Sinan Beksac   +2 more
doaj   +1 more source

Spontaneous subgaleal haemorrhage in a newborn: A rare presentation of congenital factor VII deficiency due to homogenous missense mutation of factor VII gene

Pediatric Hematology Oncology Journal, 2022
Background: Subgaleal haemorrhage (SGH) is an accumulation of blood between the aponeurosis and the periosteum following rupture of emissary veins. SGH is not uncommon in newborn with traumatic or instrumental delivery.
Ajoy Kumar Garg, Siva Chaitanya, S.K. Patnaik, Vivek Kumar   +3 more
doaj   +1 more source

Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII

The Turkish Journal of Pediatrics, 2018
Intracranial hemorrhage is considered the most common cause of death in newborns with congenital factor VII (FVII) deficiency. Recombinant activated FVII (rFVIIa) provides specific replacement therapy, however there is limited experience with its ...
Zeynep İnce, Özgül Bulut, Melike Tuğrul-Aksakal, Ayşegül Ünüvar, Ömer Devecioğlu, Asuman Çoban   +5 more
doaj   +1 more source

A viable mouse model of factor X deficiency provides evidence for maternal transfer of factor X. [PDF]

, 2008
BackgroundActivated factor X (FXa) is a vitamin K-dependent serine protease that plays a pivotal role in blood coagulation by converting prothrombin to thrombin. There are no reports of humans with complete deficiency of FX, and knockout of murine F10 is
Arruda, VR, Chu, K, Golden, JA, Herzog, RW, High, KA, Labosky, PA, Margaritis, P, Tai, SJ   +7 more
core   +2 more sources

Case of concurrent factor VII and factor XI deficiencies manifesting as spontaneous lower extremity compartment syndrome

Clinical Case Reports, 2022
Factor VII and XI deficiencies are rare bleeding disorders typically associated with mild or provoked bleeding. This case report describes a patient with factor VII and XI deficiencies with an unprovoked episode of lower extremity hematoma causing ...
Joseph P. Marshalek, David Yashar, Karen Huynh, Sarah Tomassetti   +3 more
doaj   +1 more source

Factor VII deficiency-related recurrent hemarthrosis in a female child – When to suspect?

Iraqi Journal of Hematology, 2021
Recurrent hemarthrosis is a common entity in children. Although recurrent hemarthrosis most often associated with hemophilia (VIII or IX deficiency), but rarely it can be associated with factor VII deficiency (FVIID).
Siyaram Didel, Abhishek H. L. Purohit, Deepthi Krishna, Varuna Vyas, Kuldeep Singh   +4 more
doaj   +1 more source

The Arecibo Galaxy Environment Survey VII : A Dense Filament With Extremely Long HI Streams [PDF]

, 2014
We present completed observations of the NGC 7448 galaxy group and background volume as part of the blind neutral hydrogen Arecibo Galaxy Environment Survey (AGES).
Davies, J. I., Herbst, H., Minchin, R. F., Rodriguez, R., Taylor, R., Vazquez, C.   +5 more
core   +1 more source

Obscure gastrointestinal bleeding in a patient with factor VII deficiency: a case controlled with tranexamic acid [PDF]

Pediatric Emergency Medicine Journal
Factor VII deficiency is a rare, inherited coagulopathy, which can lead to prolonged bleeding. Here, we present a case report of an adolescent with factor VII deficiency who experienced small bowel bleeding that was successfully treated with tranexamic ...
Kyu Hwa Jeong, Young Bae Choi, Yu Bin Kim   +2 more
doaj   +1 more source

Phenotypic and genotypic analysis of patients with congenital factor VII deficiency in a multicenter study in Thailand

Pediatric Hematology Oncology Journal, 2022
Objective: The phenotypic and genotypic analysis of patients with congenital factor VII deficiency were retrospectively conducted. Methods: The study included 26 patients defined as severe (n = 25) and moderate (n = 1) degree by FVII  T (38.3%), followed
Ampaiwan Chuansumrit, Surapan Parapakpenjune, Rungrote Natesirinilkul, Patcharee Komvilaisak, Werasak Sasanakul, Nongnuch Sirachainan, Anchalee Aramthienthamrong, Chorthip Wattanasutthipong, Kittima Kanchanakumhan, Kunrada Inthawong, Montana Chantaraniyom, Naonpan Pongpaothai, Nattaporntira Phalakornkul, Nisakorn Khumchan, Pacharapan Surapolchai, Panjarat Sowittayasakul, Somporn Wangruangsathit   +16 more
doaj   +1 more source

Fiona’s FVII footprint

The Journal of Haemophilia Practice, 2020
Factor VII deficiency is a rare inheritable bleeding disorder that can be challenging to manage. Blood activity levels do not correlate with bleeding risk, and prophylaxis is a more difficult treatment option than for people with haemophilia due to the ...
Mulders Greta, Tuinhout Mirjam
doaj   +1 more source