Treacher Collins syndrome is a congenital disorder of craniofacial development that has variable phenotypic expression. It can be inherited in an autosomal dominant pattern (less than 50% of cases) or can be a sporadic mutation. The hallmarks of this disease are downward-slanting palpebral fissures, mandibular hypoplasia, malar hypoplasia, coloboma of the lower eyelids, malformation of the auricular pinna, middle ear deformities, and associated conductive hearing loss. This activity reviews the evaluation and treatment of patients with Treacher Collins syndrome and highlights the role of the interprofessional team in managing patients with this condition.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/24727
- 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)
ABA - 1.0 Point; Credit Type(s): Lifelong Learning (ABA)
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, Developmental-Behavioral Pediatrics, Facial Plastic & Reconstructive Surgery, General Otolaryngology, General Pediatrics, General Surgery, Internal Medicine, Molecular Genetic Pathology, Neonatal-Perinatal Medicine, Neurodevelopmental Disabilities, Pediatric Cardiology, Pediatric Otolaryngology, Sleep Medicine
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