Review


DOI :10.26650/JARHS2019-650402   IUP :10.26650/JARHS2019-650402    Full Text (PDF)

Differential Diagnosis in Rare Coagulation Disorders

Mustafa BiliciSerap Karaman

Von Willebrand Disease (1/100,000), Hemophilia A (1/10,000) and Hemophilia B (1/30,000) account for 95-98% of bleeding disorders. Examples of rare bleeding disorders are “Platelet Diseases” and “Rare Coagulation Disorders” (RCD) which generally have a frequency of occurrence of 1/1,000,000. Due to the small number of cases, information on the epidemiology and clinical outcomes of RCDs is limited. For the same reason, it has not been possible to develop guidelines for classification and treatment. Rare factor deficiencies have similarities and differences with more well-known and common haemophilia. In this article, the differences between RCDs in the light of epidemiological data are discussed while treatment is not mentioned. 

DOI :10.26650/JARHS2019-650402   IUP :10.26650/JARHS2019-650402    Full Text (PDF)

Nadir Faktör Eksikliklerinde Ayırıcı Tanı

Mustafa BiliciSerap Karaman

Tüm kanama bozukluklarının %95-98’ini Von Willebrand Hastalığı (1/100.000), hemofili A (1/10000) ve hemofili B (1/30000) oluşturmakta, nadir rastlanan kanama bozuklukları ise trombosit hastalıkları ve “nadir faktör eksiklikleri (NFE)” olup, genel olarak 1/1.000.000 sıklıkta rastlanır. Vaka sayılarının azlığı nedeniyle NFE’nin epidemiyolojisi ve klinik sonuçları hakkındaki bilgiler sınırlıdır. Ayrıca yine aynı nedenle sınıflandırılması ve tedavisi için rehberler de geliştirilememiştir. Nadir faktör eksikliklerinin iyi bilinen ve sık görülen hemofililerle benzerlik ve farklılıkları mevcuttur. Bu yazıda epidemiyolojik veriler ışığında NFE’nin farklılıkları üzerinde durulmuş, tedaviye değinilmemiştir. 


PDF View

References

  • 1. Peyvandi, F., I. Garagiola, and E. Biguzzi, Advances in the treatment of bleeding disorders. J Thromb Haemost, 2016. 14(11): p. 2095-2106. google scholar
  • 2. Bolton-Maggs, P.H., The rare inherited coagulation disorders. Pediatr Blood Cancer, 2013. 60 Suppl 1: p. S37-40. google scholar
  • 3. Peyvandi, F., et al., Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management. Semin Thromb Hemost, 2009. 35(4): p. 349-55. google scholar
  • 4. Menegatti, M. and R. Palla, Clinical and laboratory diagnosis of rare coagulation disorders (RCDs). Thromb Res, 2019. 5. Mannucci, P.M., S. Duga, and F. Peyvandi, Recessively inherited coagulation disorders. Blood, 2004. 104(5): p. 1243-52. google scholar
  • 6. Peyvandi, F., T. Kunicki, and D. Lillicrap, Genetic sequence analysis of inherited bleeding diseases. Blood, 2013. 122(20): p. 3423-31. google scholar
  • 7. Goodeve, A.C., et al., Genetics of haemostasis. Haemophilia, 2012. 18 Suppl 4: p. 73-80. google scholar
  • 8. Palla, R., F. Peyvandi, and A.D. Shapiro, Rare bleeding disorders: diagnosis and treatment. Blood, 2015. 125(13): p. 2052-2061. google scholar
  • 9. Mumford, A.D., et al., Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors’ Organization guideline on behalf of the British Committee for Standards in Haematology. Br J Haematol, 2014. 167(3): p. 304-26. google scholar
  • 10. Peyvandi, F., M. Menegatti, and R. Palla, Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management. Semin Thromb Hemost, 2013. 39(6): p. 579-84. google scholar
  • 11. Türk Hematoloji Derneği, Nadir faktör eksiklikleri, Tanı ve tedavi klavuzu. Eylül 2013. google scholar

Citations

Copy and paste a formatted citation or use one of the options to export in your chosen format


EXPORT



APA

Bilici, M., & Karaman, S. (2019). Differential Diagnosis in Rare Coagulation Disorders. Journal of Advanced Research in Health Sciences, 2(3), 126-129. https://doi.org/10.26650/JARHS2019-650402


AMA

Bilici M, Karaman S. Differential Diagnosis in Rare Coagulation Disorders. Journal of Advanced Research in Health Sciences. 2019;2(3):126-129. https://doi.org/10.26650/JARHS2019-650402


ABNT

Bilici, M.; Karaman, S. Differential Diagnosis in Rare Coagulation Disorders. Journal of Advanced Research in Health Sciences, [Publisher Location], v. 2, n. 3, p. 126-129, 2019.


Chicago: Author-Date Style

Bilici, Mustafa, and Serap Karaman. 2019. “Differential Diagnosis in Rare Coagulation Disorders.” Journal of Advanced Research in Health Sciences 2, no. 3: 126-129. https://doi.org/10.26650/JARHS2019-650402


Chicago: Humanities Style

Bilici, Mustafa, and Serap Karaman. Differential Diagnosis in Rare Coagulation Disorders.” Journal of Advanced Research in Health Sciences 2, no. 3 (May. 2024): 126-129. https://doi.org/10.26650/JARHS2019-650402


Harvard: Australian Style

Bilici, M & Karaman, S 2019, 'Differential Diagnosis in Rare Coagulation Disorders', Journal of Advanced Research in Health Sciences, vol. 2, no. 3, pp. 126-129, viewed 19 May. 2024, https://doi.org/10.26650/JARHS2019-650402


Harvard: Author-Date Style

Bilici, M. and Karaman, S. (2019) ‘Differential Diagnosis in Rare Coagulation Disorders’, Journal of Advanced Research in Health Sciences, 2(3), pp. 126-129. https://doi.org/10.26650/JARHS2019-650402 (19 May. 2024).


MLA

Bilici, Mustafa, and Serap Karaman. Differential Diagnosis in Rare Coagulation Disorders.” Journal of Advanced Research in Health Sciences, vol. 2, no. 3, 2019, pp. 126-129. [Database Container], https://doi.org/10.26650/JARHS2019-650402


Vancouver

Bilici M, Karaman S. Differential Diagnosis in Rare Coagulation Disorders. Journal of Advanced Research in Health Sciences [Internet]. 19 May. 2024 [cited 19 May. 2024];2(3):126-129. Available from: https://doi.org/10.26650/JARHS2019-650402 doi: 10.26650/JARHS2019-650402


ISNAD

Bilici, Mustafa - Karaman, Serap. Differential Diagnosis in Rare Coagulation Disorders”. Journal of Advanced Research in Health Sciences 2/3 (May. 2024): 126-129. https://doi.org/10.26650/JARHS2019-650402



TIMELINE


Submitted25.10.2019
Accepted09.11.2019
Published Online30.12.2019

LICENCE


Attribution-NonCommercial (CC BY-NC)

This license lets others remix, tweak, and build upon your work non-commercially, and although their new works must also acknowledge you and be non-commercial, they don’t have to license their derivative works on the same terms.


SHARE




Istanbul University Press aims to contribute to the dissemination of ever growing scientific knowledge through publication of high quality scientific journals and books in accordance with the international publishing standards and ethics. Istanbul University Press follows an open access, non-commercial, scholarly publishing.