A Rare Case of Wilsons Disease with Zoophilia

P. Barman, Madhurima Khasnobis, K. Nath
{"title":"A Rare Case of Wilsons Disease with Zoophilia","authors":"P. Barman, Madhurima Khasnobis, K. Nath","doi":"10.11648/J.AJPN.20190704.11","DOIUrl":null,"url":null,"abstract":"Wilsons Disease also known as hepatolenticular degeneration is a autosomal recessive disorder, characterized by abnormal copper deposition in the liver, brain, and other tissues caused by mutation in the copper transporting gene ATP7B. Patients presents with neurological and hepatic disorder. Psychiatric manifestation are common along with movement disorder but its association with paraphilic disorders like zoophilia is very rare and there is practically no literature regarding this in North-Eatern India. In this article we report the unique case of a 21 year old boy from rural Assam suffering from Wilson’s disease with multiple neuropsychiatric manifestations among which zoophilia was noteworthy. This case report highlights a rare and atypical association between an adolescent patient of Wilson disease & zoophilia--- a relatively rare paraphilic disorder. A 21 year old boy presented in the Psychiatry emergency department in a tertiary care hospital with aggressive, disorganized behavior with reported sexual act with a cow. Examination of the patient also revealed massive organomegaly and K-F ring which on further investigation confirmed the diagnosis of Wilsons Disease. The occurrence of zoophilic behavior in Wilsons disease is very rare and we have not come across any such report regarding this. To conclude, the association between copper deposition in specific brain areas due to Wilsons disease and zoophilic behaviour we need further studies with better investigative modalities, which will in turn help in drawing an individualise treatment plan.","PeriodicalId":256299,"journal":{"name":"American Journal of Psychiatry and Neuroscience","volume":"102 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Psychiatry and Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11648/J.AJPN.20190704.11","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Wilsons Disease also known as hepatolenticular degeneration is a autosomal recessive disorder, characterized by abnormal copper deposition in the liver, brain, and other tissues caused by mutation in the copper transporting gene ATP7B. Patients presents with neurological and hepatic disorder. Psychiatric manifestation are common along with movement disorder but its association with paraphilic disorders like zoophilia is very rare and there is practically no literature regarding this in North-Eatern India. In this article we report the unique case of a 21 year old boy from rural Assam suffering from Wilson’s disease with multiple neuropsychiatric manifestations among which zoophilia was noteworthy. This case report highlights a rare and atypical association between an adolescent patient of Wilson disease & zoophilia--- a relatively rare paraphilic disorder. A 21 year old boy presented in the Psychiatry emergency department in a tertiary care hospital with aggressive, disorganized behavior with reported sexual act with a cow. Examination of the patient also revealed massive organomegaly and K-F ring which on further investigation confirmed the diagnosis of Wilsons Disease. The occurrence of zoophilic behavior in Wilsons disease is very rare and we have not come across any such report regarding this. To conclude, the association between copper deposition in specific brain areas due to Wilsons disease and zoophilic behaviour we need further studies with better investigative modalities, which will in turn help in drawing an individualise treatment plan.
罕见的威尔逊病伴动物癖1例
Wilsons病也称为肝豆状核变性,是一种常染色体隐性遗传病,其特征是铜转运基因ATP7B突变导致肝脏、脑和其他组织中铜沉积异常。患者表现为神经和肝脏紊乱。精神病学表现与运动障碍一起很常见,但它与像动物癖这样的性反常障碍的联系非常罕见,在印度东北部几乎没有关于这方面的文献。在这篇文章中,我们报告了一个来自阿萨姆邦农村的21岁男孩患有威尔逊病的独特病例,其中有多种神经精神表现,其中值得注意的是动物癖。本病例报告强调了一个罕见的和非典型的青春期Wilson病患者与动物癖之间的联系,动物癖是一种相对罕见的反性恋障碍。一个21岁的男孩出现在精神病学急诊科在三级护理医院的侵略性,混乱的行为,报告与母牛的性行为。患者的检查也发现了大量的器官肿大和K-F环,进一步调查证实了威尔逊病的诊断。威尔逊病中嗜兽行为的发生是非常罕见的,我们没有遇到任何关于这方面的报道。综上所述,威尔森病引起的特定脑区铜沉积与嗜动物行为之间的关系需要进一步的研究,这将有助于制定个性化的治疗计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信