Prader-Willi综合征的直肠脱垂和危险因素:一项基于病例的回顾。

IF 0.4 Q4 PEDIATRICS
Journal of pediatric genetics Pub Date : 2021-03-03 eCollection Date: 2022-03-01 DOI:10.1055/s-0041-1724049
Merlin G Butler
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引用次数: 1

摘要

一名14岁的Prader-Willi综合征(PWS)男性青少年患者伴母体15型体,报道了直肠脱垂,这是文献中仅有的第二例患者。在这种综合征中,直肠损伤和脱垂的易感危险因素存在,发病率一定更高,因此被低估了。这些危险因素包括皮肤和直肠撕裂、自我刺激、疼痛感觉改变、肌肉量减少、力量和体力活动减少以及胃肠(GI)紊乱。我们回顾并分析了相关文献,重点关注PWS的临床特征和行为,这些特征和行为被认为是直肠损伤和脱垂的未被充分认识的危险因素。一个说明性的情况下,提出了第二个病人报告与PWS和脱垂直肠。讨论了诱发行为和临床危险因素,包括自我刺激、直肠采摘、慢性便秘、肠道动力下降、饮水减少和限制饮食。虽然病例确实很少,但PWS中常见的身体、行为和GI表现可能导致直肠脱垂,需要对这种罕见的与肥胖相关的遗传疾病患者有更好的认识和主动监测、管理和治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prolapsed Rectum and Risk Factors in Prader-Willi Syndrome: A Case-Based Review.

A 14-year-old male adolescent patient with Prader-Willi syndrome (PWS) with maternal disomy 15 was reported with rectal prolapse as only the second patient in the literature. With predisposing risk factors present for rectal damage and prolapse in this syndrome, the incidence must be higher and therefore underreported. These risk factors include skin and rectal picking, self-stimulation, altered pain sensation, decreased muscle mass, strength and physical activity with hypotonia, and gastrointestinal (GI) disturbances. Pertinent literature was reviewed and analyzed that focused on clinical features and behavior seen in PWS as underrecognized risk factors for developing rectal damage and prolapse. An illustrative case is presented as the second patient reported with PWS and a prolapsed rectum. A discussion of predisposing behavioral and clinical risk factors is presented including for self-stimulation, rectal picking, chronic constipation, decreased gut motility, reduced water intake, and a restricted diet. Although a paucity of cases do exist, physical, behavioral, and GI findings common in PWS may contribute to rectal prolapse requiring better awareness and proactive surveillance, management, and treatment protocols for patients affected with this rare obesity-related genetic disorder.

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来源期刊
自引率
0.00%
发文量
32
期刊介绍: The Journal of Pediatric Genetics is an English multidisciplinary peer-reviewed international journal publishing articles on all aspects of genetics in childhood and of the genetics of experimental models. These topics include clinical genetics, molecular genetics, biochemical genetics, medical genetics, dysmorphology, teratology, genetic counselling, genetic engineering, formal genetics, neuropsychiatric genetics, behavioral genetics, community genetics, cytogenetics, hereditary or syndromic cancer genetics, genetic mapping, reproductive genetics, fetal pathology and prenatal diagnosis, multiple congenital anomaly syndromes, and molecular embryology of birth defects. Journal of Pediatric Genetics provides an in-depth update on new subjects and current comprehensive coverage of the latest techniques used in the diagnosis of childhood genetics. Journal of Pediatric Genetics encourages submissions from all authors throughout the world. The following articles will be considered for publication: editorials, original and review articles, short report, rapid communications, case reports, letters to the editor, and book reviews. The aim of the journal is to share and disseminate knowledge between all disciplines in the field of pediatric genetics. This journal is a publication of the World Pediatric Society: http://www.worldpediatricsociety.org/ The Journal of Pediatric Genetics is available in print and online. Articles published ahead of print are available via the eFirst service on the Thieme E-Journals platform.
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