Angioma Alliance advocates, facilitates and participates in cerebral cavernous angioma research. If you have a history of cavernous angioma, we need your help!
Angioma Alliance oversees two projects that need your participation to help drive reserach to discover a cure for Cavernous Angioma.
- The DNA/Tissue Bank provides researchers with biological samples and medical history for research projects.
- The International Cavernous Angioma Patient Registry is a communication tool that will provide you with the most up-to-date information about research projects and clinical trials that are available for participation.
Below is detailed descriptions of both programs including the link to enroll in the Patient Registry and at the bottom of this page, there is a form to begin enrollment for the DNA/Tissue Bank. Click HERE
for a side-by-side comparison of these programs.
The International Cavernous Angioma Patient Registry
If you have a history of Cavernous Angioma and are interested in research participation, please consider joining the Patient Registry. If you register you will:
- Create a profile on the Registry website and complete an online questionnaire.
- Maintain the accuracy of your profile with yearly updates.
- We will contact you about studies for which you are eligible to participate. Your information will not be shared without your permission; the Registry is simply a tool for communication about research opportunities.
To access the International Cavernous Angioma Patient Registry website, please go to:
No one knows why some cavernous angiomas hemorrhage and others do not. No one knows how to stop cavernous angiomas from hemorrhaging in the first place. Researchers are using DNA extracted from blood samples, surgically removed cavernous angioma tissue, and medical and family histories to help answer these questions. They are trying to determine if there are differences between cavernous angiomas, or between the people who have them, that can explain cavernous angioma behavior. By collecting these raw materials and distributing them to the research community, our DNA/Tissue Bank and patient registry will advance and shorten the search for a non-invasive treatment for cerebral cavernous angiomas, perhaps by years.
To learn more about research studies using the DNA/Tissue Bank resources, click HERE.
We are recruiting individuals who live in North America with a history of cavernous angiomas to participate in the DNA/Tissue Bank. Your children with cavernous angiomas are encouraged to participate if you are willing to request records and participate in the interviews.
We need your help if:
- You live in the United States or Canada
- You or your child has been diagnosed with one or more cerebral cavernous angiomas and your diagnosis has been confirmed by MRI, by genetic testing, or by pathology findings after a surgery.
- You or your affected child have had surgery to remove a cavernous angioma from your brain, spine, or skin or you have an upcoming surgery.
- You or your affected child is willing to donate a blood and cheek cell sample.
- You are willing to sign releases requesting pathology slides, medical records and imaging and participate in completing a questionnaire or interview.
- You are willing to donate your or your child’s cavernous angioma tissue if a surgery is scheduled in the future.
- You are willing to remain in contact with Angioma Alliance for a minimum of 5 years.
We are particularly seeking those who had a surgery at St. Joseph's Hospital in Phoenix, AZ since 2005 or who have a surgery planned at that facility.
Angioma Alliance DNA/Tissue Bank personnel will contact you to discuss the BioBank and answer your questions. You will be asked to sign a consent form for your or your child’s participation as well as several release forms for medical records and MRIs and for pathology slides if you or your child have had a past surgery. We will conduct an extensive interview or ask you to complete an online questionnaire about your family history, activities, and other aspects of your life.
A blood donation kit will be sent in the mail for you to take to your doctor, clinic, or blood draw center to have your or your child’s blood drawn. The kit is then mailed to a private lab where the sample is processed.
If a surgery is scheduled, the Angioma Alliance DNA/Tissue Bank will work with you, the surgeon, and the hospital to coordinate cavernous angioma tissue donation. You will need to let your surgeon know that you would like to donate your or your child's cavernous angioma to the DNA/Tissue Bank.
The Angioma Alliance DNA/Tissue Bank will follow up with you on a yearly basis to update your medical information.
If you or your child has not already had genetic testing, we will test your DNA sample for a possible CCM1, CCM2, or CCM3 mutation or CCM2 exon 2-10 deletion. If additional causative genes are identified for the illness, we will also test for mutations on these. Because the testing is done for research rather than diagnostic purposes, we can not inform you of the specific results of the testing, but we will let you know if a mutation or deletion is found. This will enable you to obtain follow-up confirmatory clinical diagnostic testing from a diagnostic laboratory. This could also mean a substantial cost savings to the you if your insurance does not cover genetic testing or if you are uninsured.
Names are removed from any samples or information that goes to researchers; only Angioma Alliance DNA/Tissue Bank staff will have access to your identifying information. Your anonymous samples will be available only to researchers whose projects have been approved by the Angioma Alliance DNA/Tissue Bank Scientific Advisory Committee. You can revoke your consent at any time and your samples and data will be recalled and destroyed.
To Begin the Enrollment Process please complete the form below. After you complete this form, you will recieve an email titled "DNA & Tissue Bank Response." If you do not recieve this note within two business days, please check you junk mail folder and/or contact Amy Akers directly at firstname.lastname@example.org