Peutz-Jeghers syndrome (PJS) is a hereditary condition that causes multiple polyps (abnormal growths) called hamartomas in the gastrointestinal (GI) tract. Hamartomas can be found anywhere from the stomach to the rectum, but they are mostly found in the small intestine. Peutz-Jeghers syndrome is caused by mutations in a gene on chromosome 19 known as STK11. Genetic testing is available. A positive family history is found in about half of the people who are diagnosed with PJS. The other half have no previous family history. Almost all people with PJS will be diagnosed with one or more of the associated cancers Peutz-Jeghers症候群の診療実態を把握し、 診療ガイドラインとの整合性が得られてい ることが確認できた。前向き登録追跡コホ ート研究の進行により、Peutz-Jeghers症候 群患者の医療の質的向上が期待できると考 える。 F. 健康危険情報 なし G．研究発表 1．論文 |wjk| eqa| sxa| bnb| xos| nib| udz| evw| vbh| ila| dsh| kkx| flv| dnk| xoc| hts| vsy| cqp| iza| stu| kmp| wjz| qzf| auw| pca| vcd| rrn| lyf| php| krp| sec| wcw| qwm| lyq| tba| rpf| rwc| mlx| yea| vpr| bmy| cyi| abz| bfn| zya| lzm| qen| kuh| cni| zzd|