Results 81 to 90 of about 5,970 (200)
Radioiodine treatment in McCune-Albright syndrome with hyperthyroidism
Indian Journal of Endocrinology and Metabolism, 2012 McCune-Albright syndrome (MAS) is a sporadic disease characterized by polyostotic fibrous dysplasia, "café-au-lait" spots and hyperfunctional endocrinopathies.
Dhritiman Chakraborty +5 more
doaj +1 more source
Taurodontism: a review on its etiology, prevalence and clinical considerations [PDF]
, 2010 Taurodontism can be defined as a change in tooth shape caused by the failure of Hertwig’s epithelial sheath diaphragm to invaginate at the proper horizontal level. An enlarged pulp chamber, apical displacement of the pulpal floor, and no constriction at
Kovvuru, Suresh Kumar, Manjunatha, B.S.
core +1 more source
Case Reports in Endocrinology, Volume 2025, Issue 1, 2025.Background: Fibrous dysplasia (FD) is a rare congenital bone disease. Denosumab, a monoclonal antibody targeting nuclear factor kappa‐B ligand (RANKL), suppresses osteoclast activity and exhibits therapeutic potential for FD. Case Presentation: We present the case of an adult female patient diagnosed with FD who had undergone 7 treatment cycles of ...
Danni Liu +5 more
wiley +1 more source
Características clínico-radiológicas orofaciais da síndrome de McCune-Albright num adulto: relato de um caso [PDF]
Fibrous dysplasia is a benign and progressive bone disease of genetic basis that can affect one or several bones. Its high incidence in the pediatric age served as a basis for it to be previously considered exclusive to this stage; however, there are ...
Morales Paz , Yanara Reyna +2 more
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Case Reports in Radiology, Volume 2025, Issue 1, 2025.Background Cherubism is a rare genetic disorder characterised by multilocular cystic lesions in the mandible and/or maxilla, which result in the typical cherub‐like face. Two forms of cherubism exist—hereditary (familial) and nonhereditary (nonfamilial)—and it usually occurs amongst children aged 2–7 years.
Seth Kwadjo Angmorterh +11 more
wiley +1 more source
Advances in Models of Fibrous Dysplasia/McCune-Albright Syndrome
Frontiers in Endocrinology, 2020 The Gs G-protein coupled receptor pathway is a critical regulator of normal bone formation and function. The Gs pathway increases intracellular cAMP levels by ultimately acting on adenylate cyclase.
Hsuan Lung +6 more
doaj +1 more source
Genomic Imprinting and Cancer: From Primordial Germ Cells to Somatic Cells [PDF]
, 2006 Imprinted genes are a subset of genes that are expressed from only one of the parental alleles. The majority of imprinted genes have roles in growth regulation and are, therefore, potential oncogenes or tumour suppressors. Cancer is a disease of aberrant
Adele Murrell
core +1 more source
McCune Albright syndrome: A case report with review of literature
Journal of Orthopedics, Traumatology and Rehabilitation, 2014 McCune Albright syndrome (MAS) is a rare disorder comprising any two of polyostotic fibrous dysplasia (PFD), café-au-lait macules and endocrine abnormalities. We present the case of a 25-year-old male who suffered a pathologic fracture of his right femur
Muhammad Haseeb +3 more
doaj +1 more source
Peripheral precocious puberty including congenital adrenal hyperplasia: causes, consequences, management and outcomes [PDF]
, 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
Caspian Journal of Internal Medicine, 2021 Background: McCune Albright syndrome (MAS) is a rare heterogeneous clinical syndrome without any predilection for ethnic group. Classic form includes triad of fibrous dysplasia, café au late spots and autonomous hyper function of one or more endocrine ...
Ali Reza Navabazam +3 more
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