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2014, Number 3

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Medisur 2014; 12 (3)

Costello syndrome. A case report

Maldonado MY, Torres MA, Duran LD
Full text How to cite this article

Language: Spanish
References: 9
Page: 516-521
PDF size: 235.73 Kb.


Key words:

costello syndrome, neurocutaneous syndromes, genetic diseases, inborn.

ABSTRACT

Costello syndrome is an extremely rare multisystem congenital disorder; only about 250 cases have been described in the literature. Its inheritance pattern is considered to be autosomal dominant, although most cases are sporadic, suggesting de novo dominant mutations. The case of a 7-year-old patient from the Frank País municipality in Holguín with clinical manifestations consistent with Costello syndrome is presented. The clinical study and description of his physical characteristics were performed, detecting as main distinctive features: storage disease-like phenotype, failure to thrive, congenital heart disease, coarse facies, mental retardation and humorous personality. Early diagnosis allows early stimulation and intervention, active screening for tumor lesions, as well as provision of genetic counselling to patients.


REFERENCES

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  2. Motosuneya T, Asazuma T, Tsuji T, Watanabe H, Nakayama Y, Nemoto K. Severe scoliosis associated with Costello syndrome: a case report. J Orthop Surg (Hong Kong). 2006 ; 14 (3): 346-9.

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Medisur. 2014;12