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ISSN 0210-5187 (Electronic)

2009, Number 3

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Med Cutan Iber Lat Am 2009; 37 (3)

McCune-Albright’s syndrome

Pitarch BG, Laguna AC, Martín GB, Febrer BM, Alegre MV

Language: Spanish
References: 11
Page: 144-146
PDF size: 192.59 Kb.


ABSTRACT

The McCune-Albright syndrome is characterized by a triad of café-au-lait macules, bone fibrous dysplasia and hyperfunctioning endocrinopathies. A nine-year-old girl with irregular café-au-lait macules on the left cheek, neck and frontal areas, as well as fibrous dysplasia of underlying bones of the skull is reported. No endocrinopathies nor precocious puberty were found.


REFERENCES

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  2. Ringel MD, Schwindinger WF, Levine MA. Clinical implications of genetic defects in G proteins. The molecular basis of McCune- Albright syndrome and Albright hereditary osteodystrophy. Medicine (Baltimore) 1996; 75: 171-84.

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