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2017, Number 1

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Cir Gen 2017; 39 (1)

McCune-Albright syndrome in an adolescent youngster

Uribe GG, Sigler ML
Full text How to cite this article 10.35366/74562

DOI

DOI: 10.35366/74562
URL: https://dx.doi.org/10.35366/74562

Language: Spanish
References: 13
Page: 37-40
PDF size: 194.61 Kb.


Key words:

McCune-Albright syndrome, adolescent male, alopecia areata.

ABSTRACT

Introduction: This is a non-hereditary, very rare syndrome, present since birth or youth; it is due to an alteration in the chromosome 20. The objective of this work is to present the case of a male adolescent who consulted because of an ulcer in the sole of the right foot; he also showed signs of this syndrome. Case report: 16-year-old male who lived in a distant rural zone; he complained of an ulcer in the sole of the right foot for several months. There was shortness of the right lower extremity, cafe-au-lait pigmented skin lesions, abnormal development of limbs and alopecia areata of the scalp. Cleaning of the ulcer, bandages, sole protector, and rest were recommended. A future work-up with X rays and consultations was planned, but he never came back. Later, he changed his address. Clinical findings were the basis of the diagnosis of McCune-Albright syndrome.


REFERENCES

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Cir Gen. 2017;39