SciELO - Scientific Electronic Library Online

 
vol.30 número1INMUNOTERAPIA CON BCG EN CARCINOMA PAPILAR DE VEJIGAQUISTE MESENTERICO COMO CAUSA DE ABDOMEN AGUDO índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Gaceta Médica Boliviana

versão On-line ISSN 1012-2966

Resumo

VILLARROEL GOYTIA, Alfredo; HOCHSTATTER ARDUZ, Erwin  e  CLAUSTRO, Roxana. SÍNDROME DE APERT (ACROCEFALOSINDACTILIA). Gac Med Bol [online]. 2007, vol.30, n.1, pp. 58-62. ISSN 1012-2966.

We report an case of newborn with Apert's syndrome. A medical literature revision was made concluding that Apert's syndrome is a congenital disease, associated with some chromosomopathies that express important cranial and facial deformities. The most important characteristics of this syndrome are fussions in some bones of the crane, hands and feet; giving the patient a characteristic aspect. It's Treatment must be multidisciplinar}' because of the multiple deformities presented in this syndrome.

Palavras-chave : Acrocephaly; syndactyly; Syndrome of Apert.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License