Doença de von Willebrand

Autores

  • Cristina João Interna de Hematologia Clínica do Instituto Português de Oncologia de Francisco Gentil, Lisboa

Palavras-chave:

factor de von Willebrand, doença de von Willebrand adquirida, pseudo doença de von Willebrand, glicoproteínas da membrana plaquetária, desmopressina, ristocetina

Resumo

A doença de von Willebrand é a doença congénita
da hemostase mais frequente na humanidade, quer
devido a alterações quantitativas do factor de von
Willebrand, quer a alterações qualitativas do mesmo.
Este trabalho apresenta uma revisão actualizada
da fisiopatologia e características clínicas desta
doença, bem como da sua classificação. São ainda
revistas a biosíntese, estrutura e funções do factor
de von Willebrand, o modo de realizar o seu
diagnóstico e as diversas opções terapêuticas são apresentadas.
O autor revê ainda a doença de von Willebran
adquirida e a pseudo-doença de von Willebrand

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Ficheiros Adicionais

Publicado

30-03-2001

Como Citar

1.
João C. Doença de von Willebrand. RPMI [Internet]. 30 de Março de 2001 [citado 17 de Novembro de 2024];8(1):28-36. Disponível em: https://revista.spmi.pt/index.php/rpmi/article/view/1893

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