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2015, Number 2

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Medisur 2015; 13 (2)

Noonan's syndrome. Case Report

Rosas HM, Rivas RED, Silva SRE
Full text How to cite this article

Language: Spanish
References: 9
Page: 316-320
PDF size: 216.39 Kb.


Key words:

Noonan syndrome, genetic diseases, inborn, diagnosis, differential.

ABSTRACT

Noonan's syndrome is a genetic, little-known disease, produced for a mutation in the 12q22 chromosome. Few data on this affection exists in Cuba; since studies with a significant sample have not been conducted that demonstrate the real frequency of the affection. An eight year old patient’s case from Banes, Holguín, is presented, to whom the syndrome through comparative technique was diagnosed, and considering the clinics and radiological characteristics. The consent of parents to do and to divulge this report was taken into account. The interest of this case consists on the low frequency of appearing of Noonan's syndrome, in fact, the first one that has been diagnosed at the municipality.


REFERENCES

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Medisur. 2015;13