TY - JOUR
T1 - A Girl with McCune-Albright Syndrome
T2 - Case Study
AU - Khairunnisa,
AU - Faizi, Muhammad
AU - Rochmah, Nur
AU - Hisbiyah, Yuni
AU - Perwitasari, Rayi Kurnia
N1 - Publisher Copyright:
© 2024 Phcogj.Com.
PY - 2024/5
Y1 - 2024/5
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85197657419&partnerID=8YFLogxK
U2 - 10.5530/pj.2024.16.119
DO - 10.5530/pj.2024.16.119
M3 - Article
AN - SCOPUS:85197657419
SN - 0975-3575
VL - 16
SP - 706
EP - 710
JO - Pharmacognosy Journal
JF - Pharmacognosy Journal
IS - 3
ER -