Hereditary and acquired ichthyosis vulgaris are cutaneous disorders of keratinization that manifest clinically by a widespread scaling of the skin. Ichthyosis vulgaris is associated with loss of function FLG gene mutations, which leads to a defective skin barrier. This activity reviews the evaluation and treatment of hereditary and acquired ichthyosis vulgaris and highlights the role of the interprofessional team in the care of patients with this condition.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/89672
- Start Date: 2023-09-01 05:00:00
- End Date: 2023-09-01 05:00:00
- Credit Details: IPCE Credits: 1.5 hours
AMA PRA Category 1 Credit™️: 1.5 hours
Nursing: 1.5 hours
Pharmacy: 1.5 hours - MOC Credit Details: ABS - 1.5 Point; Credit Type(s): Accredited CME (ABS)
ABPATH - 1.5 Point; Credit Type(s): Lifelong Learning (ABPATH)
ABIM - 1.5 Point; Credit Type(s): Medical Knowledge (ABIM)
ABS - 1.5 Point; Credit Type(s): Self-Assessment (ABS)
ABP - 1.5 Point; Credit Type(s): Lifelong Learning and Self-Assessment (ABP) - 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, Dermatopathology, Gastroenterology, General Pediatrics, General Surgery, Infectious Disease, Internal Medicine, Medical Oncology, Molecular Genetic Pathology, Pediatric Gastroenterology, Pediatric Hematology-Oncology, Pediatric Infectious Diseases
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