Cargando…

A case report of congenital factor X deficiency in an adult patient

Factor X deficiency is one of the rarest coagulation disorders representing 10% of all rare bleeding diseases with a frequency of 1:1,000,000. A 39-year-old male patient with no previous medical conditions was admitted to the hospital with a left carpal ganglion for surgical excision. Routine preope...

Descripción completa

Detalles Bibliográficos
Autores principales:	AL-Ansari, Rehab Y, Alofi, Ghufran, Aljarah, Nasser, Woodman, Alexander
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358331/ https://www.ncbi.nlm.nih.gov/pubmed/35958882 http://dx.doi.org/10.1177/2050313X221116676

Ejemplares similares

Hereditary factor XII deficiency in an adult patient: A case report
por: Al-Ansari, Rehab Y, et al.
Publicado: (2022)

“Familial Multiple Coagulation Factor Deficiencies of FXI and FXII in an Asymptomatic Saudi Woman”
por: Al-Ansari, Rehab Y., et al.
Publicado: (2023)

Severe thrombocytopenia after Vaxzevria vaccination in a single patient: A case report
por: Al-Ansari, Rehab Y, et al.
Publicado: (2022)

Impending splenic rupture as indicator of atypical chronic lymphocytic leukemia: A case report from Saudi Arabia
por: Al-Ansari, Rehab Y., et al.
Publicado: (2023)

Congenital Factor V deficiency: perioperative management (case report)
por: Fehdi, Mohamed Anass, et al.
Publicado: (2020)

Hemophagocytic lymphohistiocytosis and congenital factor VII deficiency: a case report
por: Wang, Xiong, et al.
Publicado: (2018)

Remsima (a Tumor Necrosis Factor (TNF) -α Inhibitor) induced hemolysis in a patient with Crohn's disease - Case report
por: AL-Ansari, Rehab Y., et al.
Publicado: (2021)

Congenital Limb Deficiency: A Case Report
por: Khanal, Surendra, et al.
Publicado: (2022)

Anesthesia strategy for factor X deficiency coagulopathy: case report
por: Ferreira, Carla Isabel, et al.
Publicado: (2021)

Congenital Factor X-Riyadh (Stuart-Prower) Deficiency With Isolated Prothrombin Time Prolongation: A Case Report
por: Alasmari, Badriah G, et al.
Publicado: (2023)

Isolated ten-eleven translocation 2 positive in triple negative essential thrombocythemia: Case report and literature review
por: AL-Ansari, Rehab Y, et al.
Publicado: (2021)

Diagnosis and treatment discussion of congenital factor VII deficiency in pregnancy: A case report
por: Yang, Ying, et al.
Publicado: (2021)

Recurrent miscarriage in a woman with congenital factor V deficiency: a case report
por: Shirzadi, Mohammad, et al.
Publicado: (2022)

Steroid induced hypertriglyceridemia in pregnant waman with immune thrombocytopenia – case report
por: AL-Ansari, Rehab Y., et al.
Publicado: (2022)

A young Saudi female with combined hemophagocytic lympho-histiocytosis and Kikuchi’s disease: A case report
por: Al-Zahrani, Kamal, et al.
Publicado: (2023)

Congenital Upper Limb Deficiency with Oligodactyly: A Case Report
por: Twayana, Anu Radha, et al.
Publicado: (2022)

A case of congenital factor V deficiency.
por: Song, J. W., et al.
Publicado: (1987)

Congenital Surfactant C Deficiency with Pulmonary Hypertension—A Case Report
por: Chua, Wei Chard, et al.
Publicado: (2022)

Near fatal spontaneous intraperitoneal bleeding: A rare manifestation in a congenital factor X deficiency carrier
por: Vinod, K. V., et al.
Publicado: (2015)

Perioperative management for patient with congenital factor VII deficiency who underwent laparoscopic cholecystectomy: Case report
por: Yoshimura, Tomohiro, et al.
Publicado: (2022)

Laparoscopic hepatectomy for hepatocellular carcinoma in a patient with congenital factor V deficiency: a case report
por: Seki, Takaomi, et al.
Publicado: (2022)

Successful removal of a congenital fibrovascular pupillary membrane in 2 cases with variable age at presentation and sparing of the crystalline lens
por: Al Otaibi, Abdullah, et al.
Publicado: (2023)

Pediatric split liver transplantation for congenital factor X deficiency: first 10-year follow-up of a case with portal vein stenting
por: Namgoong, Jung-Man, et al.
Publicado: (2021)

A case of intracranial hemorrhage in a neonate with congenital factor VII deficiency
por: Lee, Won Seok, et al.
Publicado: (2010)

Congenital factor XI deficiency caused by a novel F11 missense variant: a case report
por: Gotovac Jerčić, Kristina, et al.
Publicado: (2020)

Congenital surfactant protein B (SP-B) deficiency: a case report
por: Khalsi, Fatma, et al.
Publicado: (2023)

A rare case of congenital chylothorax in a Palestinian neonate
por: Abuhamda, Allam Fayez, et al.
Publicado: (2019)

Merosin-deficient congenital muscular dystrophy type 1A: A case report
por: HE, ZHANWEN, et al.
Publicado: (2013)

Ophthalmic manifestations of congenital protein C deficiency: a case report and mini review
por: Ghassemi, Fariba, et al.
Publicado: (2020)

Congenital biotinidase deficiency – MRI findings in two cases
por: Ranjan, Rahul S, et al.
Publicado: (2019)

Prostate surgery in severe congenital factor VII deficiency: A case report
por: Moussa, M., et al.
Publicado: (2018)

Acquired Factor X Deficiency without Amyloidosis Presenting with Massive Hematuria: A Case Report and Review of the Literature
por: Menakuru, Sasmith R., et al.
Publicado: (2023)

Incarcerated congenital transmesenteric hernia in an adult: a case report
por: Alhayo, Sam, et al.
Publicado: (2017)

CONGENITAL MESOBLASTIC NEPHROMA: A CASE REPORT
por: Al-Turkistani, Hatim K.
Publicado: (2008)

Management of mild congenital deficiency of Factor XI with a Factor XI inhibitor in pregnancy: A clinical case
por: Murray, Nigel P., et al.
Publicado: (2022)

Report of a rare co-incidence of congenital factor V deficiency and thalassemia intermedia in a family
por: Mourad, Yasser Abou, et al.
Publicado: (2004)

X-linked congenital adrenal hypoplasia associated with hypospadias in an Egyptian baby: a case report
por: Metwalley, Kotb Abbass, et al.
Publicado: (2012)

Case Report of Gastrointestinal Bleeding in an Adult with Chronic Visceral Acid Sphingomyelinase Deficiency
por: Cassiman, David, et al.
Publicado: (2019)

Case report of recurrent bleeding in an infant with isolated prolonged prothrombin time due to congenital factor VII deficiency---a riddle solved
por: Ganguly, Mimi, et al.
Publicado: (2022)

X-linked congenital adrenal hypoplasia: a case presentation
por: Ouyang, Hong, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_gaqtdsuf9kpm50lvb7bdv7lt6a