Incontinentia pigmenti is an X-linked dominant genodermatosis. The disease is caused by a mutation of the IKBKG gene. This rare disorder presents in the first few weeks of life. Skin lesions are typical of this disease. The eye, teeth, and central nervous system are also involved. Due to multisystemic involvement, it must be promptly diagnosed and treated. Genetic counseling plays an important part in the management. This activity reviews the evaluation and diagnosis of incontinentia pigmenti and highlights the role of the interprofessional team in evaluating and treating patients with this condition.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/140417
- Start Date: 2023-09-01 05:00:00
- End Date: 2023-09-01 05:00:00
- Credit Details: 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: Dermatopathology, General Pediatrics, General Surgery, Internal Medicine, Molecular Genetic Pathology, Neonatal-Perinatal Medicine, Pediatric Neurology, Pediatric Pathology
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