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Cerebral cavernous malformations Panel

Cerebral cavernous malformations Panel

Regular price €49.00 EUR
Regular price Sale price €49.00 EUR
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This product is only meant for customers who already purchased a MyGenome Test

Cerebral cavernomas can be sporadic or congenital. They consist of the formation of abnormal blood vessels that tend to clump and eventually break, resulting in potentially serious complications.
At the base of the cavernous malformations there are mutations in various genes coding for proteins involved in the intercellular endothelial junctions which, if altered, lead to abnormal entanglement of the capillaries. Furthermore, the lack of tight junctions between the cells is the cause of the leakage of blood components in the cavernous context itself.

This test is particularly useful for people with a family history of this type of condition or who report symptoms related to it.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.

  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • 4 genes related to hereditary forms of Cerebral cavernous malformations analyzed
  • Investigates SNP and Indel mutations up to 150 bp



See more about the product
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  • 1.

    Using a simple at home blood sample, we can collect the 100% of your DNA and analyze the genetic sequence in our lab.

  • 2.

    The sequence is divided into several parts, amplified, grouped in clusters and then sequenced.

  • 3.

    This sequencing process reveals the order of nucleotides that make up the original DNA sample.

  • 4.

    We then compare the genome with a generic and globally recognized reference DNA sequence.

Simple Blood Sample Collection

Painless, quick at home sample collection. User friendly device with CE-IVD mark and FDA approval.

Simply follow the packaging instructions and send the sample back using the pre-paid returns label.

Genomic Consultation Service

Additional reports

Check out the full range of our additional reports, available upon completion of the Genome Test.

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