Answers are grounded in this paper and cite their sources.
McCune-Albright syndrome (MAS) is a rare genetic disease characterized by skeletal, cutaneous, and endocrine system involvement. We report a 6-year-old girl with fibrous dysplasia, café-au-lait macula, and multiple hyperfunctional endocrinopathies. Treatment was palliative, the patient was planned for surgery on bilateral femur fractures and a rehabilitation program.
No takes yet. Share an insight, caveat, or question.
Khairunnisa et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: