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CCM3 Action

CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. CCM3 Action: Empower. Connect. Cure. CCM3 Action connects people affected by the ultra-rare Cerebral Cavernous Malformation 3 genetic mutation. Fewer than 100 people worldwide have been diagnosed with this genetic mutation. Our mission is to create a supportive community, provide opportunities for quality treatment, and accelerate research toward a cure. Form to contact us as soon as possible.

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Angioma Alliance

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CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. CCM3 Action: Empower. Connect. Cure. CCM3 Action connects people affected by the ultra-rare Cerebral Cavernous Malformation 3 genetic mutation. Fewer than 100 people worldwide have been diagnosed with this genetic mutation. Our mission is to create a supportive community, provide opportunities for quality treatment, and accelerate research toward a cure. Form to contact us as soon as possible.

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1 ccm3 action

2 search this site

3 ccm3 information

4 journal articles

5 known mutation list

6 printable handouts

7 our programs

8 family gatherings

9 funding research

10 talk to us

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CCM3 Action | ccm3.org Reviews

https://ccm3.org

CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. CCM3 Action: Empower. Connect. Cure. CCM3 Action connects people affected by the ultra-rare Cerebral Cavernous Malformation 3 genetic mutation. Fewer than 100 people worldwide have been diagnosed with this genetic mutation. Our mission is to create a supportive community, provide opportunities for quality treatment, and accelerate research toward a cure. Form to contact us as soon as possible.

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ccm3.org

1

CCM3 Care and Clinical Research Center - CCM3 Action

http://www.ccm3.org/programs/clinic

CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. CCM3 Care and Clinical Research Center. CCM3 Action has established a Consultation and Clinical Research Center at the University of Chicago under the direction of Dr. Issam Awad just for people who have the CCM3 mutation that causes cerebral cavernous angiomas (cavernous malformations). This Center is a place where patients can be examined so that they:. Why is it needed? What will it cost me? If your m...

2

Our Programs - CCM3 Action

http://www.ccm3.org/programs

CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. CCM3 Action intends to sponsor three primary programs. The following pages provide more information:. CCM3 Care and Clinical Research Center. At the University of Chicago coupled with the Angioma Alliance DNA/Tissue Bank provide an opportunity for quality care and increased understanding of the illness. As CCM3 Action grows, we intend to provide. Financial assistance to research.

3

For Patients and Family - CCM3 Action

http://www.ccm3.org/CCM3Info/PatientInfo

CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. For Patients and Family. CCM3 is a genetic mutation that can cause people to develop cerebral cavernous angiomas. Cerebral cavernous angiomas are blood vessel defects in the brain and spinal cord that look like mulberries. Cavernous angiomas are leaky, can grow quite large, and can cause seizures, headaches, and stroke-like symptoms. The CCM3 gene creates a protein known as PDCD10. PDCD10 is part of ...

4

CCM3 Information - CCM3 Action

http://www.ccm3.org/CCM3Info

CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. The CCM3 genetic mutation, also known as the PDCD10 mutation, is one of three mutations that can cause the hereditary form of cerebral cavernous angiomas. This section of our site provides:. For patients and families. For Patients and Family.

5

Known Mutation List - CCM3 Action

http://www.ccm3.org/CCM3Info/mutations

CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. Listed below are known human mutations in the CCM3 gene from published journal articles and other communication:. Compiled by David McDonald and Dr. Amy Akers. Deletion of entire gene. Bergametti 2005; Labauge 2006; Liquori 2007. Deletion of exon 5. C103C T; R35X. Bergametti 2005; Lee 2008. F Riant and E. Tournier-Lasserve (unpublished). C283C T; R95X. Guclu 2005, Verlaan 2005. 22C T; R108X.

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CCM3 Action: Empower. Connect. Cure. For Patients and Family. CCM3 Care and Clinical Research Center. CCM3 Action: Empower. Connect. Cure. CCM3 Action connects people affected by the ultra-rare Cerebral Cavernous Malformation 3 genetic mutation. Fewer than 100 people worldwide have been diagnosed with this genetic mutation. Our mission is to create a supportive community, provide opportunities for quality treatment, and accelerate research toward a cure. Form to contact us as soon as possible.

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