Results 61 to 70 of about 2,769 (118)
Hansen′s disease with McCune-Albright syndrome
Journal of Global Infectious Diseases, 2012 McCune-Albright syndrome (MAS) comprises a triad of fibrous dysplasia of bone, cafι-au-lait macule, and endocrinopathy. The disease is due to activating mutation of G protein-coupled receptor leading to hyperfunction of glands. Hansen′s disease is caused
KVS Hari Kumar, P Dhull, Y S Bisht
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Some aspects of precocious puberty in preschool-age girls [PDF]
РМЖ. Мать и дитя, 2022 Yu.Yu. Chebotareva1, Yu.A. Petrov1, M.A. Rodina2 1Rostov State Medical University, Rostov-on-Don, Russian Federation 2Medical Center Sem’ya, Rostov-on-Don, Russian Federation Precocious puberty (PP) remains a challenging issue for pediatrics,
Yu.Yu. Chebotareva +2 more
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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.
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Treatment of Pathological Bone Fractures in a Patient with McCune-Albright Syndrome
Case Reports in Endocrinology, 2013 McCune-Albright syndrome is a rare genetic disorder with typical skeletal and endocrine manifestations. The disease course is complicated by recurrent fractures resulting from polyostotic fibrous dysplasia and the treatment is thus primarily directed at ...
Jana Kollerova +4 more
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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
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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
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Fibrous dysplasia for radiologists: beyond ground glass bone matrix
Insights into Imaging, 2018 Fibrous dysplasia (FD) is a congenital disorder arising from sporadic mutation of the α-subunit of the Gs stimulatory protein. Osseous changes are characterised by the replacement and distortion of normal bone with poorly organised, structurally unsound,
Yevgeniya S. Kushchayeva +6 more
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Fibro-osseous lesion of maxilla. Report of two cases in a family with review of literature [PDF]
, 2011 Fibrous dysplasia is a disturbance of bone metabolism that is classified as a benign fibro-osseous lesion. Fibrous connective tissue containing abnormal bone, replaces normal bone. The etiology of fibrous dysplasia is unknown.
Kaur, Bhawandeep +2 more
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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
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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
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