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A young woman with atypical McCune–Albright syndrome and the difficult road to recovery: a case report [PDF]

Frontiers in Surgery
BackgroundFiber dysplasia is a complex condition that presents with various clinical manifestations, such as deformity, dysfunction, pathological fractures, and endocrine disorders.
Hongbin Wang, Hao Wang, Heng Liu, Xin Yang, Zhichao Meng, Yongping Cao   +5 more
doaj   +6 more sources

A case report of McCune–Albright syndrome with hepatic manifestations [PDF]

Clinical Case Reports, 2022
McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies.
Mohammad Haddadi, Elahe Lal Kheirkhah, Mojgan Ansari, Samieh Ahmadzade, Zeinab Taraz, Saeid Yazdi   +5 more
doaj   +3 more sources

Diagnostic journey for individuals with fibrous dysplasia / McCune albright syndrome (FD/MAS) [PDF]

Orphanet Journal of Rare Diseases
Background Reducing delayed diagnosis is a significant healthcare priority for individuals with rare diseases. Fibrous Dysplasia/ McCune Albright Syndrome (FD/MAS) is a rare bone disease caused by somatic activation mutations of NASA.
Kaiyang Song, Roshi Shrestha, Heather Delaney, Rohit Vijjhalwar, Alison Turner, Maria Sanchez, Muhammad Kassim Javaid   +6 more
doaj   +3 more sources

Recent research advances in pain mechanisms in McCune–Albright syndrome thinking about the pain mechanism of FD/MAS [PDF]

Journal of Orthopaedic Surgery and Research
Background The lack of effective understanding of the pain mechanism of McCune–Albright syndrome (MAS) has made the treatment of pain in this disease a difficult clinical challenge, and new therapeutic targets are urgently needed to address this dilemma.
Yong Wang, Tao Jiang
doaj   +3 more sources

Mazabraud Syndrome Associated with McCune-Albright Syndrome: A Case Report and Literature Review

Case Reports in Oncology, 2023
The Mazabraud syndrome is a rare form of bone fibrous dysplasia associated with intramuscular myxomas. The McCune-Albright syndrome is characterized by the association of dysplasia fibrous bone to one or more extra-osseous manifestations, including café ...
Laurys Boudin, Valeria De Luca, Léna Mescam-Mancini, Vincent Niziers, Delphine Perrot, Jerome Guiramand, Audrey Monneur, Christophe Chagnaud, François Bertucci   +8 more
doaj   +2 more sources

Delayed Diagnosis of McCune–Albright Syndrome [PDF]

Case Reports in Genetics, 2021
Background. McCune–Albright syndrome (MAS) is a rare heterogeneous genetic disorder that is characterized by a triad of polyostotic fibrous dysplasia (FD), café au lait spots (CAL), and multiple hyperfunctional endocrinopathies.
Bereket Fantahun, Seblewongel Desta
doaj   +2 more sources

Clinical Characteristics and Management of Patients With McCune-Albright Syndrome With GH Excess and Precocious Puberty: A Case Series and Literature Review

Frontiers in Endocrinology, 2021
BackgroundMcCune-Albright syndrome is a rare disorder characterized by fibrous dysplasia, café au lait skin spots, and hyperfunctioning endocrinopathies. The coexistence of precocious puberty and growth hormone excess in McCune-Albright syndrome is rare.
Xiao Zhai, Xiao Zhai, Lian Duan, Lian Duan, Yong Yao, Bing Xing, Kan Deng, Linjie Wang, Linjie Wang, Feng Feng, Zhiyong Liang, Hui You, Hongbo Yang, Hongbo Yang, Lin Lu, Lin Lu, Shi Chen, Shi Chen, Renzhi Wang, Hui Pan, Hui Pan, Huijuan Zhu, Huijuan Zhu   +22 more
doaj   +2 more sources

A Case of McCune–Albright Syndrome with External Auditory Canal Stenosis Treated with Image-Guided Surgery System-Assisted Temporal Bone Surgery [PDF]

Journal of International Advanced Otology
McCune–Albright syndrome is a disorder of fibrous bone dysplasia complicated by skin pigmentation and endocrine abnormalities. Although temporal bone lesions are rare, surgical treatment is required when external auditory canal (EAC) stenosis develops ...
Takaomi Kurioka, Tatsuya Takenaka, Shingo Yasutake, Yoshiaki Inuzuka, Motohiro Sato, Kunio Mizutari   +5 more
doaj   +2 more sources

Cushing syndrome as a failed cardiac screen in a patient with McCune–Albright syndrome: a case report [PDF]

Journal of Medical Case Reports, 2022
Background McCune–Albright syndrome is a complex disorder encompassing multiple endocrinopathies. These manifestations are secondary to a mutation in the stimulatory G-protein alpha subunit. Cushing syndrome is due to autonomous secretory function of the
Christy Foster, Hiba Al Zubeidi, Alicia Diaz-Thomas   +2 more
doaj   +2 more sources

Fertility journey of a patient with McCune-Albright syndrome associated with bilateral ovarian involvement [PDF]

F&S Reports
Objective: To report a patient with McCune-Albright syndrome (MAS) with bilateral ovarian involvement who had achieved a pregnancy through in vitro fertilization (IVF). Design: Case report. Setting: Academic fertility center.
Joanna J. Kim, M.D., Stephanie Dufour, M.D., Sara Awad, M.B.B.S., M.H.P.E., Bryden Magee, M.D.   +3 more
doaj   +2 more sources