Results 11 to 20 of about 2,769 (118)

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

open access: yesFrontiers in Surgery
BackgroundFiber dysplasia is a complex condition that presents with various clinical manifestations, such as deformity, dysfunction, pathological fractures, and endocrine disorders.
Hao Wang   +5 more
core   +3 more sources

Fibrous dysplasia : a tale of two syndromes [PDF]

open access: yesSouth African Journal of Radiology
DATA AVAILABILITY : The data that support the findings of this study are available on request from the corresponding author, J.F.Fibrous dysplasia (FD) is a rare, non-inherited, congenital bone disorder which may be monostotic or polyostotic.
Fourie, Jacques   +3 more
core   +3 more sources

Mc Cune Albright syndrome: gynecological perspective [PDF]

open access: yes, 2023
The key features of McCune-Albright syndrome include sexual precocious puberty, polyostotic fibrous dysplasia and café au lait spots. It is associated with hyperfunction of multiple endocrine glands.
Dharani E.   +2 more
core   +2 more sources

A case report of McCune–Albright syndrome with hepatic manifestations

open access: yesClinical 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   +5 more
doaj   +1 more source

Prophylactic intramedullary nailing of the proximal femur in a case of McCune Albright syndrome – A case report & review of literature

open access: yesJournal of Orthopaedic Reports, 2023
Introduction: Premature puberty, café-au-lait pigmentation, polyostotic fibrous dysplasia, and/or varied endocrine disorders make up the unusual condition known as McCune Albright Syndrome.
Mrinal Mahadev Kambli   +5 more
doaj   +1 more source

Polyostotic fibrous dysplasia (McCune-Albright) with rare multiple epiphyseal lesions in association with aneurysmal bone cyst and pathologic fracture

open access: yesRadiology Case Reports, 2021
Fibrous dysplasia, including McCune-Albright syndrome, is a genetic, non-inheritable benign bone disorder that may involve a single or multiple bone, typically occurring in the diaphysis or the metaphysis of long bones. In very rare instances polyostotic
Alvaro Burdiles, MD   +7 more
doaj   +1 more source

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

open access: yesFrontiers 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   +22 more
doaj   +1 more source

Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report

open access: yesEuropean Journal of Radiology Open, 2020
The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation.
Lynda N. Bile-Gui   +2 more
doaj   +1 more source

Pituitary mammosomatotroph tumor with folliculo-stellate and mucin cells in a child with McCune Albright syndrome

open access: yesHuman Pathology: Case Reports, 2019
A pituitary tumor is a common manifestation of the endocrinopathies criterion in McCune Albright syndrome. Herein, we report a 12-year-old male with McCune Albright syndrome, who presented with dysmorphic features and tall stature, then, underwent a ...
Sadeem Al-Subaie   +3 more
doaj   +1 more source

Treatment of Girls and Boys with McCune-Albright Syndrome with Precocious Puberty - Update 2017 [PDF]

open access: yes, 2017
The most common endocrinopathy associated with McCune-Albright Syndrome (MAS) is peripheral precocious puberty (PP) which occurs far more often in girls than in boys.
Eugster, Erica A., Neyman, Anna
core   +1 more source

Home - About - Disclaimer - Privacy