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2009, Number 3

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Rev Mex Pediatr 2009; 76 (3)

Sporadic Apert syndrome. A case report

Atuesta-Durán EE, Kepa BJ, Echeverri GJA, Estrada RC, López ADA, Roca KMF
Full text How to cite this article

Language: Spanish
References: 11
Page: 121-123
PDF size: 128.87 Kb.


Key words:

Apert syndrome, acrocephalosyndactyly, functional disturbances.

ABSTRACT

Apert syndrome is a form of acrocephalosyndactyly characterized for malformations of the skull, face, hands and feet. It is associated to functional disturbances related to first brachial arch. A case of boy of 14 years of age which was surgical treated for the correction or diminish the somatic abnormalities and give a better quality of life.


REFERENCES

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  5. Aleck K. Craniosynostosis syndromes in the genomic era. Semin Pediatr Neurol 2004; 11: 256-61.

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  10. Tolarova MM, Harris JA, Ordway DE, Vargervik K. Birth prevalence, mutation rate, sex ration, parents’ age, and ethnicity in Apert syndrome. Am J Med Genet 1997; 72: 394-8.

  11. Fearon JA. Treatment of the hands and feet in Apert syndrome: an evolution in management. Plast Reconstr Surg 2003; 112: 1-12.




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Rev Mex Pediatr. 2009;76