In this online, self-learning activity: Epidermolysis bullosa (EB) describes a group of rare, inherited skin diseases that are caused by mutations in at least 20 different genes with no known cure. These mutations can be inherited in an autosomal dominant or recessive manner leading to distinct clinical phenotypes. It is considered an orphan disease that affects about half a million people worldwide, with the National Epidermolysis Bullosa Registry estimating that the overall prevalence in the United States is 11.1 per one million live births.
- Provider:ScientiaCME
- Activity Link: https://www.scientiacme.org/cme-515-111-0-1-14-epidermolysis-bullosa-cme
- Start Date: 2024-02-28 06:00:00
- End Date: 2024-02-28 06:00:00
- Credit Details: AMA PRA Category 1 Credit™️: 1.0 hours
- MOC Credit Details: ABP - 1.0 Point; Credit Type(s): Lifelong Learning and Self-Assessment (ABP)
- Commercial Support: Source: Amryt Pharmaceuticals - Amount: 12475.0 - 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: General Pediatrics
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