@article {2327,
	title = {A Girl with McCune-Albright Syndrome: Case Study},
	journal = {Pharmacognosy Journal},
	volume = {16},
	year = {2024},
	month = {June 2024},
	pages = {706-710},
	type = {Case Report},
	chapter = {706},
	abstract = {<p class="rtejustify">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, caf{\'e}-au-lait macula, and multiple hyperfunctional endocrinopathies. Treatment was palliative, the patient was planned for surgery on bilateral femur fractures and a rehabilitation program.</p>
},
	doi = {10.5530/pj.2024.16.119},
	author = {Khairunnisa, Muhammad Faizi and Nur Rochmah and Yuni Hisbiyah and Rayi Kurnia Perwitasari}
}
