Rare bleeding disorders: a narrative review of epidemiology, molecular and clinical presentations, diagnosis and treatment

Rare bleeding disorders (RBDs) are a heterogeneous group of disorders including different types of coagulation factor deficiencies. The disorders are inherited in an autosomal recessive manner with different frequencies varying from 1:500000 to 1:2000000. Patients affected with RBDs are presented wi...

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Main Authors: Majid Naderi (Author), Shadi Tabibian (Author), Maryam Sadat Hosseini (Author), Shaban Alizadeh (Author), Soudabeh Hosseini (Author), Hossein Karami (Author), Hassan Mahmoodi Nesheli (Author), Akbar Dorgalaleh (Author)
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Published: Mazandaran University of Medical Sciences, 2014-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Majid Naderi  |e author 
700 1 0 |a Shadi Tabibian  |e author 
700 1 0 |a Maryam Sadat Hosseini  |e author 
700 1 0 |a Shaban Alizadeh  |e author 
700 1 0 |a Soudabeh Hosseini  |e author 
700 1 0 |a Hossein Karami  |e author 
700 1 0 |a Hassan Mahmoodi Nesheli  |e author 
700 1 0 |a Akbar Dorgalaleh  |e author 
245 0 0 |a Rare bleeding disorders: a narrative review of epidemiology, molecular and clinical presentations, diagnosis and treatment 
260 |b Mazandaran University of Medical Sciences,   |c 2014-07-01T00:00:00Z. 
500 |a 2322-4398 
500 |a 2322-4401 
520 |a Rare bleeding disorders (RBDs) are a heterogeneous group of disorders including different types of coagulation factor deficiencies. The disorders are inherited in an autosomal recessive manner with different frequencies varying from 1:500000 to 1:2000000. Patients affected with RBDs are presented with a wide spectrum of clinical manifestations ranging from mild to life threatening bleeding diathesis. These disorders are usually present in regions with high rate of parental consanguinity. Despite the rare incidence of RBDs, it is necessary for physicians to be aware of these disorders. Here we aim to have a comprehensive review on general features and also the recent advances in understanding of RBDs. MEDLINE and Web of Science databases searched for English sources from 1990 to 2014, using the following keywords: rare bleeding disorder, rare inherited disorder, factor deficiency, structure, function, epidemiology, manifestations, laboratory analysis, diagnosis, mutation, treatment, management and also all the factor deficiencies which are considered as RBD. Knowledge towards RBDs is increasing, however, most of published data are limited to small group of populations or case reports. Therefore, there are still several questions on these rare disorders which need to be clarified through large prospective studies. 
546 |a EN 
690 |a Rare Diseases 
690 |a Bleeding disorder 
690 |a Factor 
690 |a Deficiency 
690 |a Epidemiology 
690 |a Diagnosis 
690 |a Treatment 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Journal of Pediatrics Review, Vol 2, Iss 2, Pp 31-46 (2014) 
787 0 |n http://jpr.mazums.ac.ir/browse.php?a_code=A-10-255-1&slc_lang=en&sid=1 
787 0 |n https://doaj.org/toc/2322-4398 
787 0 |n https://doaj.org/toc/2322-4401 
856 4 1 |u https://doaj.org/article/ffd2f18c9ee2440fb0f7a83bb5b09da3  |z Connect to this object online.