Afibrinogenemia Report

$34.99

Afibrinogenemia

Fibrinogen is a protein of liver origin whose role is to promote blood clotting following a vascular injury. Produced at the end of the coagulation cascade, fibrinogen is converted into fibrin which, forming a network that "traps" the platelets, forms the clot that puts an end to blood loss. The congenital absence of fibrinogen or afibrinogenemia leads to the onset of hemorrhagic events of variable extent, even following minimal trauma.

3 genes analyzed


It is recommended if:

This report is indicated for those who experience signs and symptoms of congenital fibrinogen deficiency, such as bleeding gums, recurrent miscarriages, hematomas and hemarthrosis, or for those with a positive family history of this hematological condition.


List of main conditions:

  • Afibrinogenemia, congenital
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • Investigates SNP and Indel mutations up to 150 bp

Simple workflow

*To generate this report, a sequencing test is mandatory. If you have not yet acquired a sequencing test, kindly make the purchase at this link: Dante Genome Test now!

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FAQs

How will my data be used?

Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.

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You will be provided with a digital version of the raw data and reports. Thanks to these in-depth tools, you will be able to share your preferred information with your geneticist and/or doctor to indicate and plan the healthiest course for you. 

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*Raw data will be available free of charge for the first 30 days after release.

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