Results 61 to 70 of about 2,181,916 (247)

Fibrous dysplasia and the McCune-Albright syndrome: various aspects of a heterogeneous disease [PDF]

open access: yes, 2021
In this thesis various aspects of fibrous dysplasia/the McCune-Albright syndrome (FD/MAS) are presented.
Hagelstein-Rotman, M.
core   +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  

Persistent Diabetes Mellitus Postadrenalectomy in Neonatal McCune-Albright Syndrome [PDF]

open access: goldGlobal Pediatric Health, 2017
Mustafa Tosur MD   +5 more
doaj   +2 more sources

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  

Genotype-phenotype correlation in fibrous dysplasia/McCune-Albright syndrome.

open access: yesJournal of Clinical Endocrinology and Metabolism, 2021
CONTEXT Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) is a rare bone and endocrine disorder resulting in fractures, pain, and disability. There are no targeted or effective therapies to alter the disease course.
M. Zhadina   +5 more
semanticscholar   +1 more source

McCune-Albright syndrome

open access: yesRheumatology, 2011
McCune-Albright syndrome (MAS) is a very rare disease characterizedby the triad of bone defects, skin hyperpigmentation, andvarious types of endocrine and non-endocrine manifestations.
Juraj Payer   +6 more
doaj   +2 more sources

Peripheral precocious puberty including congenital adrenal hyperplasia: causes, consequences, management and outcomes [PDF]

open access: yes, 2019
Peripheral precocious puberty results from peripheral production of sex steroids independent of activation of the hypothalamic-pituitary gonadal axis. It is much less common than central precocious puberty.
Eugster, Erica A., Haddad, Nadine G.
core   +1 more source

Oral manifestations of McCune-Albright syndrome

open access: yesIndian Journal of Endocrinology and Metabolism, 2013
McCune- Albright Syndrome (MAS) is a rare fibrosseous lesion, characterized by a classic triad of polyostotic fibrous dysplasia (PFD), cafι -au-lait macules (CALM) and underlying endocrinopathies.
Konidena Aravinda   +2 more
doaj   +1 more source

Clinical Case of Mccune-Albright-Braitsev Syndrome (MAS)

open access: yesМедицинский вестник Юга России, 2023
The presented clinical case describes orphan disease known as MAS with manifested symptoms of precocious puberty, recurrent ovarian cysts, fibrous dysplasia, café-au-lait skin pigmentation and abnormal cardiac conduction. The pathogenesis is based on the
F. V. Valeeva   +4 more
doaj   +1 more source

Surgical treatment of femoral deformities in polyostotic fibrous dysplasia and McCune-Albright syndrome: A literature review

open access: yesWorld Journal of Orthopaedics, 2022
BACKGROUND Surgical correction of femoral deformities in polyostotic fibrous dysplasia (PFD) or McCune-Albright syndrome (MAS), such as coxa vara or shepherd’s crook deformity, is a challenge.
G. Gorgolini   +5 more
semanticscholar   +1 more source

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