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McCune-Albright syndrome. Report of a male patient
The Turkish Journal of Pediatrics, 1965 N Bilginturan
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1987
The McCune Albright syndrome is characterized in complete form by (a) patchy areas of a particular type of progressive bone disease termed polyostotic fibrous dysplasia; (b) multiple areas of cutaneous light brown pigmentation or cafe au lait spots; and (c) autonomous hyperfunction of one or more of the endocrine system, especially the gonads and ...
M, Danon, J D, Crawford
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The McCune Albright syndrome is characterized in complete form by (a) patchy areas of a particular type of progressive bone disease termed polyostotic fibrous dysplasia; (b) multiple areas of cutaneous light brown pigmentation or cafe au lait spots; and (c) autonomous hyperfunction of one or more of the endocrine system, especially the gonads and ...
M, Danon, J D, Crawford
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JAMA, 1986
This article describes clinical follow-up of 15 patients—13 females and two males—with McCune-Albright syndrome. Osseous fractures occurred only during childhood, while hearing impairment due to temporal bone involvement occurred in four of six adults.
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This article describes clinical follow-up of 15 patients—13 females and two males—with McCune-Albright syndrome. Osseous fractures occurred only during childhood, while hearing impairment due to temporal bone involvement occurred in four of six adults.
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McCune-Albright Syndrome with Thyrotoxicosis
Clinical Nuclear Medicine, 2001The authors report a rare case of McCune-Albright syndrome in a 5-year-old boy with thyrotoxicosis resulting from a hyperfunctioning solitary thyroid nodule shown on a Tc-99 thyroid scan. He also had an associated elevated parathyroid hormone level. Since 1963, only 34 cases of McCune-Albright syndrome with hyperthyroidism have been described.
A K, Singh +4 more
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Journal of Pediatric Endocrinology and Metabolism, 2007
Alan, Daneman, Denis, Daneman
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Alan, Daneman, Denis, Daneman
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Journal of the National Medical Association, 1982
A case of polyostotic fibrous dysplasia, cutaneous pigmentation, and a bifid ureter is presented. The need for urinary tract investigation in McCune-Albright's syndrome is stressed.
A A, Laditan +3 more
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A case of polyostotic fibrous dysplasia, cutaneous pigmentation, and a bifid ureter is presented. The need for urinary tract investigation in McCune-Albright's syndrome is stressed.
A A, Laditan +3 more
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