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Related to McCune-Albright syndrome: neurofibromatosis, Carney complex, Silver-Russell syndrome
MÄSMünchner Ägyptologische Studien (German: Munich Egyptologist Studies; book)
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References in periodicals archive ?
Long-term outcomes of letrozole treatment for precocious puberty in girls with McCune-Albright syndrome. Eur J Endocrinol 2016:175:477-483.
Capan, "Anesthetic considerations in McCune-Albright syndrome: Case report with literature review," Anesthesia & Analgesia, vol.
Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.
Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med.
Hyperthyroidism with fibrous dysplasia: an unusual presentation of McCune-Albright syndrome. Exp Clin Endocrinol Diabetes 2007; 115 : 331-3.
Hypersecretion of growth hormone and prolactin in McCune-Albright syndrome. J Clin Endocrinol Metab 1998; 68: 1148-54.
Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome. Proc Natl Acad Sci U S A 1992;89:5152-5156.
McCune-Albright Syndrome (MAS) is a considerably rare syndrome in which hyperthyroidism, hyperparathyroidism, hypercortisolism, excessive secretion of growth hormone and prolactin may be observed in addition to the three classical findings (1, 2).
Congenital diseases that are characterized by a thin frontal bone cortex--such as McCune-Albright syndrome (5) and osteogenesis imperfecta (6)--can lead to dilation of the frontal sinuses.
While the majority of the girls received a diagnosis of idiopathic pubertal development, 12% of them had additional endocrine diagnoses, including neurofibromatosis, McCune-Albright syndrome, growth hormone deficiency, hypothyroidism, congenital adrenal hyperplasia, pituitary microadenoma, and hyperinsulinism.
McCune-Albright Syndrome Division of the MAGIC Foundation 3167 Greensburg Rd N Canton, OH 44720 (216) 896-4455 1,4,6,10