Leber hereditary optic neuropathy (LHON) is a rare mitochondrial disorder that typically presents in young males with progressive visual loss due to optic neuropathy. Highlighting the pioneering connection of LHON with mitochondrial DNA point mutations and its maternal inheritance pattern, this activity encompasses comprehensive insights into evaluating and managing this condition. It reviews diagnostic approaches, therapeutic interventions, and emerging research, offering clinicians a robust understanding of LHON’s clinical manifestations and the latest advancements in its treatment landscape.Emphasizing the role of the interprofessional team, the activity underscores the collaborative efforts required to optimize care delivery and enhance outcomes for individuals afflicted by LHON. The course discussion covers interdisciplinary strategies, fostering a holistic approach to address the multifaceted challenges of managing this rare mitochondrial disorder, aiming to equip healthcare professionals with updated knowledge and comprehensive strategies to improve patient care.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/24145
- 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) - 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, General Surgery, Internal Medicine, Molecular Genetic Pathology