Albright hereditary osteodystrophy (AHO) is a hereditary condition due to inactivating GNAS1 gene mutation. AHO is characterized by a round face, short stature with a stocky habitus, brachydactyly, subcutaneous ossification, and dental anomalies. AHO may be associated with hormonal resistance in patients with pseudohypoparathyroidism type 1A and 1C and is often the first clue for their diagnosis. In addition, one or more features of the AHO phenotype may be present in other disorders which should be distinguished from AHO. This activity highlights the role of the interprofessional team in the diagnosis and management of patients with Albright hereditary osteodystrophy.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/17327
- 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)
ABOS - 1.0 Point; Credit Type(s): Accredited CME (ABOS)
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) - 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, Clinical Pathology, Endocrine, Endocrinology, Diabetes, and Metabolism, General Pediatrics, General Surgery, Hospice and Palliative Medicine, Molecular Genetic Pathology, Pediatric Endocrinology, Pediatric Orthopaedic Surgery, Pediatric Rheumatology, Rheumatology, Soft Tissue & Bone
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