Indirect Molecular Diagnosis of Congenital Factor Χ І І І Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms (Review Article)

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Shahraki Hojat; Fathi Majid; TABIBIAN SHADI; Sargazi Aval Omolbanin; Mollanoori Hasan; ZAKER FARHAD; TEIMOURIAN SHAHRAM; Daneshi Maryam; DORGALALEH AKBAR

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Journal: IRANIAN JOURNAL OF PEDIATRIC HEMATOLOGY AND ONCOLOGY Year:2020 | Volume:10 | Issue:2 Page(s): 114-130

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Title

Indirect Molecular Diagnosis of Congenital Factor Χ І І І Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms (Review Article)

Author(s)

Keywords

Factor XIII deficiency

Molecular Diagnostic Techniques

Microsatellite Repeats

Polymorphism

Abstract

Background: Congenital factor XIII (FXIII) deficiency is one of the rarest bleeding disorders with a prevalence of one per 2 million in the general population. The disorder is accompanied by a high rate of life-threatening bleeding. Due to normal results of routine coagulation tests, diagnosis of the disorder is challenging, but molecular methods can be used for precise diagnosis. Direct mutation detection is the standard method for confirmation of the disorder, but indirect molecular diagnosis can be used as a fast and cost-benefit choice. In the present study, we described indirect molecular methods for molecular diagnosis of congenital FXIII deficiency. Materials and Methods: For this study, a comprehensive literature review was performed on PubMed, Embase, Web of Science, and Scopus databases using the following keywords: “ indirect molecular diagnosis” with “ rare bleeding disorder” , “ coagulation factor XIII/13 deficiency” , “ prenatal diagnosis” “ rare bleeding disorder” , “ molecular diagnosis” , “ factor XIII/13 deficiency” , “ indirect molecular diagnosis” “ carrier detection” , and “ factor XIII/13” . These words were used separately and in combination with each other. Results: A total of 293 papers were founded, among them 67 papers were selected for the study. Indirect molecular diagnostic approach can be done using candidate microsatellites and single nucleotide Polymorphisms (SNP). This method can be used for prenatal diagnosis and carrier detection, especially in the areas with low economic resources. Polymorphic genetic markers associated with F13 gene like HumFXIII01, HumFXIIIA02, HumFXIIIB, rs7740009, and rs3024405 SNPs can be used for indirect molecular diagnosis of congenital FXIII deficiency. Finally, by comparing patient’ s polymorphic markers with healthy individuals, diagnosis can be made. Conclusion: It seems that indirect molecular diagnosis is a relatively reliable and cost-effective method for diagnosis of congenital FXIII deficiency in the areas with low economic resources.

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APA: Copy

Shahraki, Hojat, Fathi, Majid, TABIBIAN, SHADI, Sargazi Aval, Omolbanin, Mollanoori, Hasan, ZAKER, FARHAD, TEIMOURIAN, SHAHRAM, Daneshi, Maryam, & DORGALALEH, AKBAR. (2020). Indirect Molecular Diagnosis of Congenital Factor Χ І І І Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms (Review Article). IRANIAN JOURNAL OF PEDIATRIC HEMATOLOGY AND ONCOLOGY, 10(2), 114-130. SID. https://sid.ir/paper/969055/en

Vancouver: Copy

Shahraki Hojat, Fathi Majid, TABIBIAN SHADI, Sargazi Aval Omolbanin, Mollanoori Hasan, ZAKER FARHAD, TEIMOURIAN SHAHRAM, Daneshi Maryam, DORGALALEH AKBAR. Indirect Molecular Diagnosis of Congenital Factor Χ І І І Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms (Review Article). IRANIAN JOURNAL OF PEDIATRIC HEMATOLOGY AND ONCOLOGY[Internet]. 2020;10(2):114-130. Available from: https://sid.ir/paper/969055/en

IEEE: Copy

Hojat Shahraki, Majid Fathi, SHADI TABIBIAN, Omolbanin Sargazi Aval, Hasan Mollanoori, FARHAD ZAKER, SHAHRAM TEIMOURIAN, Maryam Daneshi, and AKBAR DORGALALEH, “Indirect Molecular Diagnosis of Congenital Factor Χ І І І Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms (Review Article),” IRANIAN JOURNAL OF PEDIATRIC HEMATOLOGY AND ONCOLOGY, vol. 10, no. 2, pp. 114–130, 2020, [Online]. Available: https://sid.ir/paper/969055/en

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