Síndrome de Sturge-Weber: relato de caso clínico

@inproceedings{Costa2004SndromeDS,
  title={S{\'i}ndrome de Sturge-Weber: relato de caso cl{\'i}nico},
  author={Jos{\'e} Renato Costa and Robson Almeida de Rezende and Daniela Nascimento Silva and M{\'a}rcia Cristina Caetano Leite and Ivana Calmon Motta and Gustavo Negri Bandeira de Mello},
  year={2004}
}
  • José Renato Costa, Robson Almeida de Rezende, +3 authors Gustavo Negri Bandeira de Mello
  • Published 2004
  • DOI:10.21722/rbps.v2i1.10684
The Sturge-Weber disease is a few condition of development, not hereditary featured of harmatomatous vascular proliferation, involve the tissues of brain and face. Characterized by corticocerebral angiomatosis, brain calcification, epilepsy, ocular alterations, mental retardation and facial nevus with color of wine port in the face.The aim of this work is shown the principal features of the Sturge-Weber syndrome in one patient with bilateral nevus in the face and scalp. To be commented clinical… CONTINUE READING

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