International SMA Patient Registry

This project is supported by CureSMA (http://curesma.org/).

The Registry functions as a liaison between patients and families interested in participating
in research and researchers interested in studying SMA. The Registry contains information
from 2,500 families and over 3,000 individuals with SMA from all over the world and continues
to grow.

The Registry has helped recruit participants for clinical trials and has provided data for
important SMA research studies. The Registry helps centralize information on this rare
genetic disease, provides families a way to learn about research studies and provides
researchers a way to find research participants.

Individuals and families affected by SMA are invited to join the Registry. Participants are
asked to complete questionnaires about the symptoms, treatment, medications, and other
experiences with SMA. Visit the Participant Portal for more information on how to sign up for
the Registry.

Participant information is stored in a secure database. Researchers who are interested in
studying SMA can request two types of data from the Registry, de-identified information and
identifiable information. De-identified information does not contain any names or personal
identifiers, and can be given to researchers without having to contact Registry families.
Identifiable information includes information that can identify you and will never be
released without getting your written permission to do so. Identifiable information includes
data such as names and dates of birth. Some researchers may also request contact with
families to obtain specific information or to request participation in a research study. In
these instances, the Registry will contact each potential participant to ask if they are
willing to share their identifiable information for a research project.

The Registry recognizes the importance of global collaboration. Working together with
researchers from all over the world is very important in the investigation of SMA. In 2008
the Registry joined the group, Translational Research in Europe for the Assessment and
Treatment of Neuromuscular Diseases (TREAT-NMD) in a global collaboration to further the
research goals of the neuromuscular disease community. TREAT-NMD has developed a global
database that compiles deidentified data transferred from participating registries around the
world. The main objective of the TREAT-NMD database is to assess the feasibility of clinical
trials, to facilitate the planning of clinical trials and to support the enrollment of
patients in clinical trials. This international database will also be used to answer
questions regarding the prevalence of particular neuromuscular disorders and assessing the
support of other activities such as assessing standards of care and diagnosis.

Inclusion Criteria:

- Individuals or family members of individuals who have been diagnosed with SMA.