黑斑息肉综合征(Peutz-Jeghers syndrome, PJS)又称家族性黏膜皮肤色素沉着胃肠道息肉病,是一种常染色体显性遗传病,以皮肤黏膜色素沉着、胃肠道多发息肉为主要特点。患病率为1/200000～1/8000。患者胃肠道息肉发生癌变风险较高,需要定期监测、规律随诊、及时治疗。黑斑息肉综合征是一种常染色体显性遗传疾病,大部分与...
Peutz-Jeghers syndrome is an uncommon genodermatosis. The clinical and radiological features of Peutz-Jeghers syndrome are described in a 12-year-old male child. The relevant literature is briefly reviewed.doi:10.1159/000251286B.S.N. Reddy
Peutz-Jeghers syndrome Pexeva See More Nearby Entries Cite this Entry Style “Peutz-Jeghers syndrome.” Merriam-Webster.com Medical Dictionary, Merriam-Webster, https://www.merriam-webster.com/medical/Peutz-Jeghers%20syndrome. Accessed 16 Dec. 2024. Copy Citation Share...
波伊茨-耶格 综合征 波伊茨-耶格综合征(Peutz-Jeghers syndrome,PJS),也被称为黑斑息肉综合征,是常染色体显性遗传的综合征,是一类伴有黏膜、皮肤色素沉着的全胃肠道多发性息肉病。2018年5月该疾病被列入国家卫生健康委员会等5部门联合制定的《第一批罕见病目录...
网络释义 1. 黑斑息肉综合征 黑斑息肉综合征(Peutz-Jeghers Syndrome)潘铨 龚汉石 【摘要】:正 黑斑息肉综合征可发生一定并发症,常因认识不足而误诊 … www.cnki.com.cn|基于15个网页 2. 黑斑息肉病 ...瘤的诊断和治疗,并对我国遗传性非息肉病性结直肠癌、黑斑息肉病(Peutz-Jeghers syndrome)进行致病基因检...
Sign up with one click: Facebook Twitter Google Share on Facebook polyp (redirected fromPeutz-Jeghers syndrome) Thesaurus Medical Acronyms Encyclopedia Wikipedia Related to Peutz-Jeghers syndrome:Lynch syndrome,Turcot syndrome polyp pedunculate polyp (top) and sessile polyp (bottom) in a section of ...
Peutz-Jeghers syndrome (PJS) is characterized by the association of gastrointestinal polyposis and mucocutaneous pigmentation. Peutz-Jeghers-type hamartomatous polyps are most common in the small intestine (in order of prevalence: in the jejunum, ileum, and duodenum) but can also occur in the stomac...
Peutz-Jeghers综合征(peutz-jeghers syndrome,PJS)是一类少见的以胃肠道多发性息肉和黏膜黑斑为临床表现的综合征。病因尚不完全清晰,临床表现主要以消化道症状和皮肤黏膜色素沉着为主。诊断主要依靠患者临床表现及辅助检查。内镜检查常可发现胃肠道多发性息肉,基因检测常可发现丝氨酸/苏氨酸激酶11(serine/threonine kinase...
T. (2010). Medical management update: Peutz Jeghers syndrome. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 109, 5–11. CrossRef Jeghers, H., Mc, K. V., & Katz, K. H. (1949). Generalized intestinal polyposis and melanin spots of the oral mucosa, ...
Peutz-Jeghers syndrome is autosomal dominant, meaning that the mutation that causes it is not on one of the sex-linked chromosomes (X and Y) and that one copy of the defective gene, received from either parent, is enough to cause the disorder. The genetic defect can also arise in someone...