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The objective of our study was to assess the effectiveness of our reference center since its constitution.
In a retrospective cohort study, we compared the activity of our center, including the time elapsed between diagnosis and access to the center and the diagnostic delay of patients with fibrous dysplasia between two periods, 1996-2006 (before certification of our center) and 2007-2019 (after certification of our center).
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Inclusion criteria
We have included children and adults with FD/MAS who visited at least once in our center (outpatient and hospitalized patients). The diagnosis was established by an expert of the center, based on clinical, biological, imaging and/or histological arguments
Exclusion criteria
The absence of detectable bone lesion
528 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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