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KMID : 0381219720040030203
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Journal of RIMSK
1972 Volume.4 No. 3 p.203 ~ p.206
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A CASE REPORT OF McCUNE-ALBRIGHT´S SYNDROME
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Abstract
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McCune-Albright´s syndrome is manifested by the association of polyostotic fibrous dysplasia, cutaneous pigmentation and endocrine dysfunction.
The authors experienced a 9-year-old girl with McCune-Albright´s syndrome. Cutaneous pigmentation began in infancy, polyostotic fibrous dysplasia and precocious puberty started 4 years later. Recently, she suffered from the typical lion face, limping gait, whitish vaginal discharge and a mild degree of mental retardation.
The diagnosis was established by characteristic clinical features, radiologic evidence, biochemical assay, and bone biopsy findings.
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KEYWORD
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