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Clinical and genetic findings in patients with spinobulbar muscular atrophy (SBMA or Kennedy disease)

Neurological Disorders

In this study we will recruit people who have SBMA (or are carriers) and collect health information. We will collect DNA and RNA samples for genetic analysis. We will interact with communities. Participants are encouraged to help guide the study by joining meetings with the study team.

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Conditions de participation

  • Sexe:

    Male, Female, Intersex

  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:
Diagnosis of SBMA (Kennedy disease), or carrier of the Kennedy disease mutation
Age >18
Exclusion Criteria:
Children, and those who cannot provide written informed consent, are not eligible to participate.

Lieu de l'étude

University of Calgary
University of Calgary
Calgary, Alberta
Canada

Contactez l'équipe d'étude

Étude parrainée par
University of Calgary
Participants recherchés
Plus d'informations
ID de l'étude: REB21-0901