Results 1 to 10 of about 133 (116)

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   +3 more sources

Congenital Factor VII Deficiency Presenting with Isolated Recurrent Hematuria: A Case Report

Acta Medica Iranica, 2021
Introduction: Factor VII deficiency is a rare congenital coagulopathy disorder. In most cases this disorder is diagnosed in childhood. Common symptoms of congenital factor VII deficiency are different and consist of mucosal cutaneous hemorrhage ...
Shahla Ansary Damavandi, Maryam Shamspour, Neda Ashayery, Milad Ahmadi Marzaleh   +3 more
doaj   +1 more source

Congenital factor VII deficiency: When to suspect?

Pediatric Hematology Oncology Journal, 2016
Ankit Ranjan, Sushma Malik, Poonam Wade, Purvi Kadakia   +3 more
doaj   +2 more sources

A case of intracranial hemorrhage in a neonate with congenital factor VII deficiency [PDF]

Korean Journal of Pediatrics, 2010
Congenital factor VII deficiency is a rare autosomal-recessive bleeding disorder. Bleeding manifestations and clinical findings vary widely, ranging from asymptomatic subjects to patients with hemorrhages that may cause significant handicaps.
Won Seok Lee, Young Sil Park
doaj   +1 more source

Inhibitors to factor VII in congenital factor VII deficiency [PDF]

Haemophilia, 2014
We performed a prospective study of FVII inhibitor occurrence in a large number of patients with FVII deficiency who had received replacement therapy for spontaneous or traumatic bleeding episodes, major or minor surgical interventions or prophylaxis.Inhibitor development was detected in 2.6% (3/115) of patients, but the incidence of de novo inhibitors
Batorova A, Mariani G, Kavakli K, de Saez AR, Caliskan U, Karimi M, PINOTTI, Mirko, Napolitano M, Dolce A, Sørensen B, Ingerslev J, STER Study Group   +11 more
openaire   +3 more sources

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

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

Congenital factor VII deficiency presenting first time as isolated recurrent hematuria at late age

Saudi Journal of Kidney Diseases and Transplantation, 2019
Hematological conditions rarely present as isolated hematuria. Factor VII deficiency is a rare congenital coagulopathy inherited as autosomal recessive pattern. It usually presents a severe life-threatening bleeding at an early age.
Suman Sethi, Sudhir Mehta, Nitin Sethi, Vikas Makkar, Simran Kaur, Manpreet Kaur Jhingar   +5 more
doaj   +1 more source

Aortic valve and coronary artery bypass surgery in a patient with factor VII deficiency

Annals of Cardiac Anaesthesia, 2021
Congenital factor VII (FVII) deficiency is a rare bleeding disorder (RBD) with phenotypes ranging from asymptomatic state to life threatening bleeding episodes. There is no established recommendation for the perioperative management of patients scheduled
Larissa Henze, Christian Junghanss, Alper Öner, Pascal M Dohmen, Anthony Alozie   +4 more
doaj   +1 more source

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   +1 more source