ArticleViewAbstractPharmacognosy Journal,2024,16,3,706-710.DOI:10.5530/pj.2024.16.119Published:June 2024Type:Case ReportA Girl with McCune-Albright Syndrome: Case StudyKhairunnisa Muhammad Faizi, Nur Rochmah, Yuni Hisbiyah, and Rayi Kurnia Perwitasari Khairunnisa, Muhammad Faizi*, Nur Rochmah,Yuni Hisbiyah, Rayi Kurnia Perwitasari Department of Child Health, Faculty of Medicine, Universitas Airlangga/Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA. 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. View:PDF (657.43 KB) PDF Images ‹ Challenges in the Diagnosis and Management of Congenital Adrenal Hyperplasia: A Case Report up Ganglion Impar Block and Neurolysis for Perineal Pain in Anal Adenocarcinoma: A Case Report ›