Lipoid proteinosis is an autosomal recessive condition characterized by hyaline-like deposits in the skin, mucous membranes, and other parts of the body. It is caused by a mutation in the extracellular matrix 1 (ECM1) gene. This activity reviews the evaluation and management of lipoid proteinosis and highlights the role of the interprofessional team in improving care for patients with this condition.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/129466
- Start Date: 2023-09-01 05:00:00
- End Date: 2023-09-01 05:00:00
- Credit Details: AMA PRA Category 1 Credit™️: 1.0 hours
Nursing: 1.0 hours
Pharmacy: 1.0 hours - MOC Credit Details: ABS - 1.0 Point; Credit Type(s): Accredited CME (ABS)
ABPATH - 1.0 Point; Credit Type(s): Lifelong Learning (ABPATH)
ABIM - 1.0 Point; Credit Type(s): Medical Knowledge (ABIM)
ABS - 1.0 Point; Credit Type(s): Self-Assessment (ABS)
ABP - 1.0 Point; Credit Type(s): Lifelong Learning and Self-Assessment (ABP)
ABOHNS - 1.0 Point; Credit Type(s): Self-Assessment (ABOHNS) - Commercial Support: No
- Activity Type: Enduring Material
- CME Finder Type: Online Learning
- Fee to Participate: Variable
- Measured Outcome: Learner Knowledge, Learner/Team Competence
- Provider Ship: Directly Provided
- Registration: Open to all
- Specialty: Adolescent Medicine, Chemical Pathology, Cytopathology, Dermatopathology, Gastroenterology, General Otolaryngology, General Pediatrics, General Surgery, Internal Medicine, Laryngology, Molecular Genetic Pathology, Neuropathology (incl. Neuromuscular), Pediatric Gastroenterology, Pediatric Neurology
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