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    • Home
    • Our Mission
      • Founder & Inspiration
      • Financials
      • Contact Us
    • Work with Us
      • Board of Directors
      • Scientific Advisory Board
      • Board of Volunteers
      • Professional Testimonials
      • Family Testimonials
      • SpecialEngagements/Media
    • Support us
      • Donations
      • Shop Merchandise
    • Events
      • Fishing Tournaments
    • Research
      • VAMP2 Syndrome
    • Resources
      • Support Groups
      • Webinars
  • Home
  • Our Mission
    • Founder & Inspiration
    • Financials
    • Contact Us
  • Work with Us
    • Board of Directors
    • Scientific Advisory Board
    • Board of Volunteers
    • Professional Testimonials
    • Family Testimonials
    • SpecialEngagements/Media
  • Support us
    • Donations
    • Shop Merchandise
  • Events
    • Fishing Tournaments
  • Research
    • VAMP2 Syndrome
  • Resources
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VAMP2 Syndrome

Point of Contact

  

Head of Patient Advocacy Group & Founder of vamp2.org


Alexandra Gaudlap 

Agaudlap@ragingraymondfoundation.org

research updates

VAMP2 Syndrome Awareness Day

First Awareness Day: August 4, 2024

Will be held annually.

Gene Therapy

VAMP2 is a likely candidate for gene therapy

 

-Gene therapy is a treatment that introduces new genetic material into a person’s cells to modify or manipulate the expression of a gene product or alter the biological properties of living cells to treat or cure disease.


- Gene therapy makes use of safe virus’s called Adeno Associated Virus (AAV) which is used as a vehicle to transport the VAMP2 gene therapy to the patient’s cells


- A number of gene therapies are now approved for other

genetic disorders and available for therapeutic use eg Zolgensma® for the treatment of Spinal Muscular Atrophy.


- There are more than 4,000 gene therapy clinical trials in

various phases of development

Presented by Dr. Wendy Gold from CMRI - Sydney, Australia

Download PDF

Presented by University College of London & Yale University

A collaborative international research team from University College London (UCL) and Yale University

 

Professors Kirill Volynski and Dimitri Kullmann of the UCL Queen Square Institute of Neurology, in partnership with Dr. Shyam Krishnakumar from Yale School of Medicine's Department of Neurology, have received a 4- year project grant from the Medical Research Council (part of UK Research and Innovation) to study neurodevelopmental disorders caused by VAMP2 mutations. 


Project summary:

Recent years have seen the discovery of genetic mutations underlying many neurodevelopmental diseases, which, although individually rare, collectively account for a substantial burden to individuals, their families and society. How these mutations result in learning disability, autism, speech problems, and epilepsy is gradually emerging, prompting the search for new treatments to mitigate the symptoms. However, there is an important group of disorders for which the consequences of the mutations at the microscopic level remain very poorly understood: these disorders are caused by mutations that affect how neurons signal to other neurons or muscle cells. Such signalling takes place at synapses and is fundamental for all brain functions, as well as the control of movements and the function of many other organs. At the core of synaptic communication is the precise discharge of packets of chemical messengers (neurotransmitters). We now have a highly detailed understanding of how the so-called SNARE proteins assemble to bring these packets, known as synaptic vesicles, to the membrane and then discharge the neurotransmitter into the synaptic cleft upon arrival of an electrical signal. We refer to the neurodevelopmental disorders caused by defects of SNAREs and functionally associated proteins collectively as ‘SNAREopathies’.


The goal of our proposal is to understand how these defects alter the discharge of neurotransmitters from synaptic vesicles and the consequences for brain circuit function and also investigate whether these effects could potentially be reversed by harnessing powerful new tools for genetic therapy.


An especially difficult challenge for many SNAREopathies is that they are suspected of acting in a genetically dominant manner. That is, if only one of the two copies of the gene encoding a SNARE protein carries a mutation, it may suppress the function of the entire SNARE protein complex, including the normal, unaffected copy of the gene. We have chosen to focus exclusively on mutations of a gene that encodes the essential SNARE protein known as vesicle-associated membrane protein 2, or VAMP2.


Our proposal brings together complementary expertise. We are able to characterize the molecular machinery of SNARE proteins by stripping neurotransmitter vesicle trafficking down to the essential steps of assembly of VAMP2 with its partners and the detailed rearrangements that occur upon the arrival of a signal to discharge the vesicle contents. We will combine this approach with highly sensitive measurements of how precisely neurotransmitter is released at individual synapses and how this process is affected by different VAMP2 mutations. We will also address the consequences for the function of small neuronal circuits in a mouse model carrying a human mutation. Finally, guided by a quantitative understanding of how many copies of each of the key molecules interact to support normal vesicle trafficking, we will design a therapy aimed at rescuing the effects of the mutation, and ask which aspects of the disease are potentially amenable to rescue in the mouse model: if the therapy is delivered once symptoms have manifested,  can we only suppress seizures, or can we also improve learning and other defects which might have arisen during early development before symptom onset?


The proposed research will provide much-needed clarity on the mechanisms of VAMP2 mutations, build towards a viable treatment option that can be translated to the clinic in due course, and define a research pipeline that can be applied to other SNAREopathies.

 

Professor Kirill Volnyski

Professor Kirill Volnyski

Professor Kirill Volnyski

Dr. Dimitri Kullmann

Professor Kirill Volnyski

Professor Kirill Volnyski

Dr. Shyam Krishnakumar

Professor Kirill Volnyski

Dr. Shyam Krishnakumar

Presented by Genomics England

Download PDF

A Mom's Journey to her Son's Diagnosis of VAMP2 Syndrome

Chapter 1

Karen discovers that her son, George, has a significant healthcare challenge 

Chapter 2

 Karen has a consultation with consultant geneticist 

Chapter 3

 

 Sample arrival at Illumina Laboratory Services

 

Chapter 4

 

DNA Sequencing at Illumina Laboratory Services

 

Chapter 5

 

Karen's family's genomes are analyzed 

 

Chapter 6

 

Karen's family's genomes are interpreted for a genomic cause

 

Chapter 7

 

Karen and Meriel discuss the genomic findings for George

 

Chapter 8

 

Karen uses her family's diagnosis to reach out to families around the world

 

Register with Patient & Family Contact Registry

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Join our Private Facebook Group for VAMP2 Patients & Families

This Facebook group is for patients and families of VAMP2 Syndrome Patients only. 

Join Group

Join Simon's Searchlight

What is Simon's Searchlight?

 

Raging Raymond Foundation is partnering with Simons Searchlight to help advance research on VAMP2-related syndrome. Simons Searchlight is an online international research program, building an ever-growing natural history database, biorepository, and resource network of over 185 rare genetic neurodevelopmental disorders.


By joining their community and sharing your experiences, you contribute to a growing database used by scientists worldwide to advance the understanding of your genetic condition. Through online surveys and optional blood sample collection, they gather valuable information to improve lives and drive scientific progress. Families like yours are the key to making meaningful progress.


To register for Simons Searchlight, go to the Simons Searchlight website at www.simonssearchlight.org and click “Join Us.”



Here are resources provided by Simon's Searchlight to support our rare and growing community.

 

 

  • VAMP2 webpage

 

  • VAMP2 Gene Guide

VAMP2 SYndrome Warriors

EIN - 92-0324693

Copyright © 2023 Raging Raymond Foundation  

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