Review highlights the need for diverse multiethnic cohorts with biosampling in fibromuscular dysplasia, indicating the importance of patient advocacy in guiding clinical research.
Longitudinal cohort studies of individuals of multiple ethnicities with biosampling are needed to better understand the risk factors, pathophysiological features, and outcomes of FMD. Patient advocacy groups could assist researchers in answering patient-centered questions regarding FMD.
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Touzé et al. (2018) studied this question.
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