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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. 


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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 (Dec. 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 22 Dec. 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 (22 Dec. 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]. 22 Dec. 2024 [cited 22 Dec. 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 (Dec. 2024): 126-129. https://doi.org/10.26650/JARHS2019-650402



TIMELINE


Submitted25.10.2019
Accepted09.11.2019
Published Online30.12.2019

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