StudyFinder
Tissue biopsies for the study of FSHD
Recruiting
A single visit study with muscle and/or skin biopsy / blood draw, performed to determine whether a molecular or cellular defect can be attributed to cells of FSHD muscle. This study is recruiting both individuals with genetically confirmed FSHD as well as unaffected healthy (control) individuals.
Not specified
Inclusion Criteria:
• Genetic confirmation of Fascioscapulohumeral Muscular Dystrophy (FSHD)
• at least 4 years old
• Healthy Family Members: parent or sibling of someone who has FSHD
Exclusion Criteria:
• heart failure, respiratory insufficiency that requires respiratory support
• taking anticoagulants or anti platelet medications (aspirin or NSAIDs)
Rare Diseases, Heart & Vascular
Clinics and Surgery Center (CSC), Fascioscapulohumeral Muscular Dystrophy (FSHD)
Ana Mitanoska - mitan001@umn.edu
Michael Kyba
STUDY00000409
20277