The first reported case of factor X deficiency in a Filipino child – case study

1. Othman T, Abdelkarim A, Huynh K, Uche A, Lee J. Inherited moderate factor X deficiency presenting as cardiac tamponade. Case Rep Hematol 2019; 2019: 9657516. doi: 10.1155/2019/9657516. Othman T Abdelkarim A Huynh K Uche A Lee J . Inherited moderate factor X deficiency presenting as cardiac tamponade . Case Rep Hematol 2019 ; 2019 : 9657516 . doi: 10.1155/2019/9657516 . Open DOISearch in Google Scholar

2. National Bleeding Disorders Foundation. Factor X: An overview of symptoms, genetics, and treatments to help you understand factor X deficiency. Available from: https://www.hemophilia.org/bleeding-disorders-a-z/types/other-factor-deficiencies/factor-x (accessed 15 September 2023). National Bleeding Disorders Foundation . Factor X: An overview of symptoms, genetics, and treatments to help you understand factor X deficiency . Available from: https://www.hemophilia.org/bleeding-disorders-a-z/types/other-factor-deficiencies/factor-x ( accessed 15 September 2023 ). Search in Google Scholar

3. Petkova J, Friedman KD. (2014). Other congenital coagulopathies. In: McQueen CA (ed.). Comprehensive Toxicology, 3rd edn. Volume 12: Hematopoeic System Toxicology. Elsevier, 2018: 337-347. doi: 10.1016/B978-0-08-100601-6.00067-3. Petkova J Friedman KD . ( 2014 ). Other congenital coagulopathies . In: McQueen CA (ed.). Comprehensive Toxicology , 3rd edn. Volume 12 : Hematopoeic System Toxicology. Elsevier , 2018 : 337 - 347 . doi: 10.1016/B978-0-08-100601-6.00067-3 . Open DOISearch in Google Scholar

4. Peyvandi F, Menegatti M. Treatment of rare factor deficiencies in 2016. Hematology Am Soc Hematol Educ Program 2016; 2016(1): 663-669. doi:10.1182/asheducation-2016.1.663. Peyvandi F Menegatti M . Treatment of rare factor deficiencies in 2016 . Hematology Am Soc Hematol Educ Program 2016 ; 2016 ( 1 ): 663 - 669 . doi: 10.1182/asheducation-2016.1.663 . Open DOISearch in Google Scholar

5. National Organization for Rare Disorders. (2021). Factor X deficiency. Last updated 6 June 2023. Available from https://rarediseases.org/rare-diseases/factor-x-defíciency/ (accessed 15 September 2023). National Organization for Rare Disorders . ( 2021 ). Factor X deficiency. Last updated 6 June 2023 . Available from https://rarediseases.org/rare-diseases/factor-x-defíciency/ ( accessed 15 September 2023 ). Search in Google Scholar

6. World Federation of Hemophilia. Report on the Annual Global Survey 2021. 2022. Available from: https://www1.wfh.org/publications/fíles/pdf-2324.pdf (accessed 15 September 2023). World Federation of Hemophilia . Report on the Annual Global Survey 2021 . 2022 . Available from: https://www1.wfh.org/publications/fíles/pdf-2324.pdf ( accessed 15 September 2023 ). Search in Google Scholar

7. Neuenschwander PF. COAGULATION CASCADE | Factor X. Encyclopedia of Respiratory Medicine. Academic Press, 2006: 499-503. doi: 10.1016/B0-12-370879-6/00085-5. Neuenschwander PF . COAGULATION CASCADE | Factor X . Encyclopedia of Respiratory Medicine . Academic Press , 2006 : 499 - 503 . doi: 10.1016/B0-12-370879-6/00085-5 . Open DOISearch in Google Scholar

8. Brown MA, Stenberg LM, Stenflo J. Chapter 642 – Coagulation Factor Xa. In: Rawlings ND, Salvesen G (eds). Handbook of Proteolytic Enzymes, 3rd edn. Academic Press, 2013: 2908–2915. doi: 10.1016/B978-0-12-382219-2.00642-6. Brown MA Stenberg LM Stenflo J . Chapter 642 – Coagulation Factor Xa . In: Rawlings ND Salvesen G (eds). Handbook of Proteolytic Enzymes , 3rd edn. Academic Press , 2013 : 2908 – 2915 . doi: 10.1016/B978-0-12-382219-2.00642-6 . Open DOISearch in Google Scholar

9. Garmo C, Bajwa T, Burns B. Physiology, Clotting Mechanism. [Updated 2022 Sep 5]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK507795/ (accessed 15 September 2023). Garmo C Bajwa T Burns B . Physiology, Clotting Mechanism . [Updated 2022 Sep 5] . In: StatPearls [Internet] . Treasure Island (FL) : StatPearls Publishing ; 2023 Jan -. Available from: https://www.ncbi.nlm.nih.gov/books/NBK507795/ ( accessed 15 September 2023 ). Search in Google Scholar

10. Venkatesh S, Ross C, Ramkumar V. Severe factor X deficiency in pregnancy. – an obstetric challenge. Int J Pregnancy & Child Birth 2017; 2(1): 14-15. doi: 10.15406/ipcb.2017.02.000008. Venkatesh S Ross C Ramkumar V . Severe factor X deficiency in pregnancy. – an obstetric challenge . Int J Pregnancy & Child Birth 2017 ; 2 ( 1 ): 14 - 15 . doi: 10.15406/ipcb.2017.02.000008 . Open DOISearch in Google Scholar

11. Gailani D, Wheeler AP, Neff AT. Chapter 137 – Rare coagulation factor deficiencies. In: Hoffman R, Benz EJ, Silberstein LE, et al. (eds). Hematology, 7th edn. Elsevier, 2018: 2034-2050. doi: 10.1016/B978-0-323-35762-3.00137-2. Gailani D Wheeler AP Neff AT . Chapter 137 – Rare coagulation factor deficiencies . In: Hoffman R Benz EJ Silberstein LE (eds). Hematology, 7th edn. Elsevier , 2018 : 2034 - 2050 . doi: 10.1016/B978-0-323-35762-3.00137-2 . Open DOISearch in Google Scholar

12. Tarantino MD. Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency. Haemophilia 2021; 27(4): 531-543. doi:10.1111/hae.14223. Tarantino MD . Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency . Haemophilia 2021 ; 27 ( 4 ): 531 - 543 . doi: 10.1111/hae.14223 . Open DOISearch in Google Scholar

13. Al-Rahal NK. Inherited bleeding disorders in Iraq and consanguineous marriage. Int J Hematol Oncol Stem Cell Res 2018; 12(4): 273-281. Al- Rahal NK . Inherited bleeding disorders in Iraq and consanguineous marriage . Int J Hematol Oncol Stem Cell Res 2018 ; 12 ( 4 ): 273 - 281 . Search in Google Scholar

14. Brown DL, Kouides PA. Diagnosis and treatment of inherited factor X deficiency. Haemophilia 2008; 14: 1176-1182. doi: 10.1111/j.1365-2516.2008.01856.x. Brown DL Kouides PA . Diagnosis and treatment of inherited factor X deficiency . Haemophilia 2008 ; 14 : 1176 - 1182 . doi: 10.1111/j.1365-2516.2008.01856.x . Open DOISearch in Google Scholar

15. Nance D, Josephson NC, Paulyson-Nunez K, James A. Factor X deficiency and pregnancy: preconception counselling and therapeutic options. Haemophilia 2012; 18(3): e277-85. doi: 10.1111/j.1365-2516.2011.02724.x. Nance D Josephson NC Paulyson-Nunez K James A . Factor X deficiency and pregnancy: preconception counselling and therapeutic options . Haemophilia 2012 ; 18 ( 3 ): e277-85 . doi: 10.1111/j.1365-2516.2011.02724.x . Open DOISearch in Google Scholar

16. Chatterjee T, Philip J, Nair V, et al. Inherited factor X (Stuart-Prower Factor) deficiency and its management. Med J Armed Forces India 2015; 71(Suppl 1): S184-S186. doi:10.1016/j. mjafi.2014.01.007 Chatterjee T Philip J Nair V Inherited factor X (Stuart-Prower Factor) deficiency and its management . Med J Armed Forces India 2015 ; 71 ( Suppl 1 ): S184 - S186 . doi: 10.1016/j.mjafi.2014.01.007 Open DOISearch in Google Scholar

17. Peyvandi F, Auerswald G, Austin SK, et al. Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency. Blood Rev 2021; 50: 100833. doi: 10.1016/j.blre.2021.100833. Peyvandi F Auerswald G Austin SK Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency . Blood Rev 2021 ; 50 : 100833 . doi: 10.1016/j.blre.2021.100833 . Open DOISearch in Google Scholar

18. Roberts HR, Escobar MA. Chapter 5 – Less common congenital disorders of hemostasis. In: Kitchens CS, Konkle BA, Kessler CM (eds). Consultative Hemostasis and Thrombosis, 2nd edn. W.B. Saunders, 2007. Roberts HR Escobar MA . Chapter 5 – Less common congenital disorders of hemostasis . In: Kitchens CS Konkle BA Kessler CM (eds). Consultative Hemostasis and Thrombosis, 2nd edn. W.B. Saunders , 2007 . Search in Google Scholar

19. Liesner R, Akanezi C, Norton M, Payne J. Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high-purity plasma-derived factor X (pdFX) concentrate. Haemophilia 2018; 24(6): 941-949. doi: 10.1111/hae.13500. Liesner R Akanezi C Norton M Payne J . Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high-purity plasma-derived factor X (pdFX) concentrate . Haemophilia 2018 ; 24 ( 6 ): 941 - 949 . doi: 10.1111/hae.13500 . Open DOISearch in Google Scholar

20. National Bleeding Disorders Foundation. FDA approves Coagadex^®, first factor X concentrate. 21 October 2015. Available from: https://www.hemophilia.org/news/fda-approves-coagadexr-first-factor-x-concentrate (accessed 15 September 2023). National Bleeding Disorders Foundation . FDA approves Coagadex^®, first factor X concentrate . 21 October 2015 . Available from: https://www.hemophilia.org/news/fda-approves-coagadexr-first-factor-x-concentrate ( accessed 15 September 2023 ). Search in Google Scholar

21. Obermann K, Jowett M, Kwon S. The role of national health insurance for achieving UHC in the Philippines: a mixed methods analysis. Glob Health Action 2018; 11(1): 1483638. doi: 10.1080/16549716.2018.1483638. Obermann K Jowett M Kwon S . The role of national health insurance for achieving UHC in the Philippines: a mixed methods analysis . Glob Health Action 2018 ; 11 ( 1 ): 1483638 . doi: 10.1080/16549716.2018.1483638 . Open DOISearch in Google Scholar