A case of hereditary hemorrhagic telangiectasia / 소아과
Korean Journal of Pediatrics
;
: 1018-1023, 2007.
Artigo
em Inglês
| WPRIM
| ID: wpr-128437
ABSTRACT
Hereditary hemorrhagic telagiectasia (HHT), which is characterized by the classic triad of mucocutaneous telangiectases, arteriovenous malformations (AVMs) and inheritance, is an autosomal dominant disorder. The characteristic manifestations of HHT are all due to abnormalities of the vascular structure. This report deals with the case of a 14-year-old girl with typical features of HHT that include recurrent epistaxis, mucocutanous telangiectases, pulmonary and cerebral AVMs and a familial occurrence.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Malformações Arteriovenosas
/
Recidiva
/
Telangiectasia Hemorrágica Hereditária
/
Telangiectasia
/
Testamentos
/
Epistaxe
/
Padrões de Herança
Limite:
Adolescente
/
Feminino
/
Humanos
Idioma:
Inglês
Revista:
Korean Journal of Pediatrics
Ano de publicação:
2007
Tipo de documento:
Artigo
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