Advances in Study on Pathogenesis and Treatment of Peutz-Jeghers Syndrome / 胃肠病学
Chinese Journal of Gastroenterology
; (12): 492-495, 2014.
Artigo
em Chinês
| WPRIM (Pacífico Ocidental)
| ID: wpr-456776
Biblioteca responsável:
WPRO
ABSTRACT
Peutz-Jeghers syndrome ( PJS ) is a rare autosomal dominant inherited disease characterized by mucocutaneous pigmentation and multiple gastrointestinal polyposis. Recent studies suggested that mutation in STK11 gene on chromosome 19p13. 3 was considered as the major cause of PJS. In this paper,we summarized the clinical features, pathogenesis,diagnosis and treatment of PJS through literature review.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo de etiologia
Idioma:
Chinês
Revista:
Chinese Journal of Gastroenterology
Ano de publicação:
2014
Tipo de documento:
Artigo