Clinical and genetic findings in patients with spinobulbar muscular atrophy (SBMA or Kennedy disease)
Summary
In this study we will recruit people who have SBMA (or are carriers) and collect health information. We will collect DNA samples for genetic analysis. We will interact with communities. Participants are encouraged to help guide the study by joining meetings with the study team.
Eligibility
Eligible gender: Male, Female, Transgender, Other
Eligible ages: 18 to 100
Inclusion criteria:
Diagnosis of SBMA (Kennedy disease), or carrier
Age >18
Exclusion criteria:
Children, and those who cannot provide written informed consent, are not eligible to participate.
Participate
Fill out the following form if you want to participate in this research
Collection of personal information
Your personal information is collected under
the authority of section 33(c) of the Freedom of Information and Protection of Privacy Act. If
you have any questions about the collection or use of this information, please visit our
Access to Information page.
Additional information
Contact information
Gerald Pfeffer
Principal investigator:
Gerald Pfeffer
Clinical trial:
No
REB-ID:
REB21-0901