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  3. Farmasi
  4. Jurnal Internasional
  5. Pharmacognosy Journal
  6. VOL 16 NO 3 2024
Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/8598
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dc.contributor.authorKhairunnisa, Khairunnisa-
dc.contributor.authorFaizi, Muhammad-
dc.contributor.authorRochmah, Nur-
dc.contributor.authorHisbiyah, Yuni-
dc.contributor.authorKurnia Perwitasari, Rayi-
dc.date.accessioned2024-11-29T04:27:34Z-
dc.date.available2024-11-29T04:27:34Z-
dc.date.issued2024-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/8598-
dc.description.abstractMcCune-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 programen_US
dc.titleA Girl with McCune-Albright Syndrome: Case Studyen_US
dc.typeArticleen_US
Appears in Collections:VOL 16 NO 3 2024

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