A Girl with McCune-Albright Syndrome: Case Study

Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/8598

Title:	A Girl with McCune-Albright Syndrome: Case Study
Authors:	Khairunnisa, Khairunnisa Faizi, Muhammad Rochmah, Nur Hisbiyah, Yuni Kurnia Perwitasari, Rayi
Issue Date:	2024
Abstract:	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
URI:	http://localhost:8080/xmlui/handle/123456789/8598
Appears in Collections:	VOL 16 NO 3 2024

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