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Test Code 124

Cerebral Cavernous Malformations via the CCM2 Gene, Exons 2-10 Deletion

CCM2

3 weeks (STAT 2 weeks)

Who is this test for?
  • Individuals for whom prior genetic testing was negative or detected a single variant associated with autosomal recessive disease in the relevant gene, and clinical suspicion is high for disease caused by that particular gene
  • Family members of patients who have tested positive for one of these particular deletions/duplications/inversions
Method
Targeted PCR
Specimen(s)

Blood, Buccal, Saliva, Tissue

Order Options

OTHER OPTIONS
for pricing.

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