In this online, self-learning activity:
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare genetic connective tissue disorder characterized by dysregulated chondrogenesis, with heterotopic ossification (HO) being the most typical feature. The global prevalence of FOP is estimated at 1.43 per million individuals, with a U.S. prevalence of 0.88 per million. FOP develops due to a mutation in the ACVR1 gene encoding the active receptor-like kinase (ALK2), with unique presenting symptoms including great toe malformations and the development of swelling in several areas of the body within the first decade of life.
- Provider:ScientiaCME
- Activity Link: https://www.scientiacme.org/cme-482-111-0-1-18-fop-cme
- Start Date: 2023-04-14 05:00:00
- End Date: 2023-04-14 05:00:00
- Credit Details: AMA PRA Category 1 Credit™️: 1.25 hours
- MOC Credit Details: ABIM - 1.25 Point; Credit Type(s): Medical Knowledge (ABIM)
ABP - 1.25 Point; Credit Type(s): Lifelong Learning and Self-Assessment (ABP) - Commercial Support: Source: Ipsen - Amount: 22450.0 - Is Kind Support: False
- Activity Type: Enduring Material
- CME Finder Type: Online Learning
- Fee to Participate: No, it's free
- Measured Outcome: Learner Competence, Learner Knowledge, Learner Performance
- Provider Ship: Directly Provided
- Registration: Open to all
- Specialty: Endocrinology, Diabetes, and Metabolism, General Pediatrics, Internal Medicine, Pediatric Endocrinology
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