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- Objective To investigate the surgical treatment of familial adenomatous polyposis(FAP). 目的 探讨家族性腺瘤样息肉病 (familialadenomatouspolyposis ,FAP)的外科治疗。
- Severe dysplasia in children with familial adenomatous polyposis:Rare or simply overlooked? 家族性腺瘤样息肉病患儿的重度不典型增生:是否罕见或仅是被忽略
- As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant. 家族性腺瘤息肉病的遗传方式是常染色体显性遗传。
- The conditions were familial adenomatous polyposis, myotonic dystrophy, multiple endocrine neoplasia, hereditary motor and sensory neuropathy. 这些疾病包括家族腺瘤息肉
- Objective To assess the clinical efficacy of sulindac on familial adenomatous polyposis (FAP) and its possible mechanism. 目的 观察舒林酸对家族性腺瘤息肉病 (FAP)的临床疗效 ,并探讨其可能的作用机制。
- The APC gene was identified in 1991 at chromosome 5 q 21. which is responsible for the familial adenomatous polyposis (FAP). APC基因是1991年被发现的一类肿瘤抑制基因,它被定位于人第5号染色体5q21处。
- Conclusion: Congenital hypertrophy of retinal pigment epithelium (CHRPE) associated with familiar adenomatous polyposis has been described before. 结论：家族性大肠肉症之肠胃道以外的临床表现，以视网膜色素上皮肥大为常见之病灶。
- Objective:To discuss the value of congenital hypertrophy retinal pigment epithelium(CHRPE) in diagnosis of familial adenomatous polyposis(FAP). 目的:探讨先天性视网膜色素上皮细胞肥大(CHRPE)在家族性腺瘤性息肉病诊断中的意义。
- Objective: To discuss the value of congenital hypertrophy retinal pigment epithelium (CHRPE) in diagnosis of familial adenomatous polyposis (FAP). 摘要目的：探讨先天性视网膜色素上皮细胞肥大(CHRPE)在家族性腺瘤性息肉病诊断中的意义。
- Familial adenomatous polyposis (FAP) is an inherited condition in which numerous polyps form mainly in the epithelium of the large intestine. 什么是'家族性腺瘤性息肉-继承条件多生长在大肠癌'?
- The authors reported their retrospective analysis of peri-operation n ursing of 8 patients with familial adenomatous polyposis after panproctocolectom y under abdominoscope. 笔者回顾分析8例家族性腺瘤性息肉病病人经腹腔镜下全结肠直肠切除术治疗的围手术期护理。
- Objective To evaluate long term outcome of ileal pouch anal anastomosis(IPAA )and ileorectal anastomosis(IRA) in patients with familial adenomatous polyposis(FAP). 目的探讨家族性腺瘤性息肉病采用回肠贮袋肛管吻合术与回肠直肠吻合术两种术式的手术效果。
- All the cases were confirmed by histopathologic examination, including 13 cases of patients with single or multiple polyps and 10 cases of adenomatous polyposis. 全部病例均经病理组织学检查证实，伴单发或多发性息肉13例，其中腺瘤性息肉10例。
- Methods Eight cases including 5 ulcerative colitis and 3 familial adenomatous polyposis treated with this surgical procedure between 1990 to 2000 were retrospectively reviewed. 方法回顾性总结1990年以来进行的8例保留回盲瓣之全结肠切除、直肠粘膜剥除,盲肠经直肠肌鞘肛管吻合患者,其中溃疡性结肠炎患者5例,家族性腺瘤性息肉病患者3例。
- To explore a new therapeutic method of high frequency e1ectric cutting under colonoscope and its clinical efficacy in treatment of familial adenomatous polyposis(FAP). 结论结肠镜下高频电切治疗家族性腺瘤性息肉病,结合定期结肠镜随访的方案安全可行,近期疗效满意。
- The protein truncation test was to be established for analyzing mutations in the adenomatous polyposis coli (APC) gene which play an important role in familial adenomatous polyposis (FAP). 摘要 建立蛋白截短检测技术，分析家族性腺瘤样息肉病（FAP）发病相关基因APC基因的胚系突变，研究基因突变型与FAP疾病表型的关系。
- Methods 159 of 106 cases of colorectal polyps by electronic high-frequency electric knife colon endoscopic treatment effi cacy analysis,including adenomatous polyposis 85,accounting for 53.5 percent. 方法对106例159枚大肠息肉经电子结肠镜下高频电刀治疗的疗效进行分析;其中腺瘤性息肉85枚;占53.;5%25。
- Purpose:To study the early molecular pathological changes in 14 adenomas of 10 familial adenomatous polyposis (FAP)patients. 目的 :研究来自 10个家族性多发性肠息肉症 (FAP)患者 14个腺瘤的早期分子病理学变化。
- Colorectal adenomatous polyposis (FAP) 家族性腺瘤性息肉病
- Attenuated colorectal adenomatous polyposis (AFAP) 衰减型家族性腺瘤性息肉病
