May-Hegglin anomaly (MHA) is a rare autosomal dominant disease characterized by neutrophils with abnormal cytoplasmic inclusions, large platelets, and variable thrombocytopenia. May-Hegglin anomaly is a member of a group of diseases associated with myosin heavy chain single gene defects that represent hereditary forms of macrothrombocytopenia associated with leukocyte inclusions and variable clinical features such as sensorineural hearing loss, presenile cataracts, and renal failure. This group also includes Fechtner syndrome, Sebastian syndrome, and Epstein syndrome. This activity describes the pathophysiology, etiology, presentation and treatment of May-Hegglin anomaly and highlights the role of the interprofessional team in providing care for affected individuals.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/24793
- 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: General Otolaryngology, General Surgery, Hematology, Hematology (Blood, BM), Hematopathology (LN, Spleen), Molecular Genetic Pathology, Nephrology, Neurotology, Pediatric Hematology-Oncology, Pediatric Nephrology, Pediatric Otolaryngology