Carnitine Deficiency in a Patient with Shapiro Syndrome

P. Yager, Maria Alkhasova, D. Rudy
{"title":"Carnitine Deficiency in a Patient with Shapiro Syndrome","authors":"P. Yager, Maria Alkhasova, D. Rudy","doi":"10.35248/2165-8048.19.9.312","DOIUrl":null,"url":null,"abstract":"Spontaneous hyperhidrosis with hypothermia and agenesis of the corpus callosum is known as Classical Shapiro Syndrome (CSS) and was first reported by Shapiro and Plum in 1967. We report a well-documented case of a 39-yearold woman with SS diagnosed at the age of 5-years-old who was diagnosed with Carnitine deficiency at 30-years-old. This is the first reported case of SS with Carnitine deficiency, which was treated with levocarnitine. Our patient also carries with her several comorbid diagnoses which have been reported in other cases of SS. These include primary amenorrhea (untreated), primary hypothyroidism (treated with levothyroxine and liothyronine), seizure disorder (treated with lamotrigine, levetiracetam, and eslicarbazepine acetates), and hypothermia-induced cytopenia (resolved with the addition of liothyronine). Additionally, this case offers unique insights gained from longitudinal care.","PeriodicalId":92650,"journal":{"name":"Internal medicine: open access","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Internal medicine: open access","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35248/2165-8048.19.9.312","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Spontaneous hyperhidrosis with hypothermia and agenesis of the corpus callosum is known as Classical Shapiro Syndrome (CSS) and was first reported by Shapiro and Plum in 1967. We report a well-documented case of a 39-yearold woman with SS diagnosed at the age of 5-years-old who was diagnosed with Carnitine deficiency at 30-years-old. This is the first reported case of SS with Carnitine deficiency, which was treated with levocarnitine. Our patient also carries with her several comorbid diagnoses which have been reported in other cases of SS. These include primary amenorrhea (untreated), primary hypothyroidism (treated with levothyroxine and liothyronine), seizure disorder (treated with lamotrigine, levetiracetam, and eslicarbazepine acetates), and hypothermia-induced cytopenia (resolved with the addition of liothyronine). Additionally, this case offers unique insights gained from longitudinal care.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
夏皮罗综合征患者肉碱缺乏症
自发性多汗症伴低体温和胼胝体发育不全被称为经典夏皮罗综合征(CSS),由夏皮罗和梅在1967年首次报道。我们报告了一个有充分文献记载的病例,一名39岁的女性在5岁时被诊断为SS,她在30岁时被诊断为肉碱缺乏症。这是第一例报道的左旋肉碱缺乏症的SS,用左卡尼汀治疗。本例患者还伴有其他SS病例报告的合并症诊断,包括原发性闭经(未经治疗)、原发性甲状腺功能减退(用左甲状腺素和碘甲状腺原氨酸治疗)、癫痫发作(用拉莫三嗪、左乙拉西坦和醋酸埃斯卡巴西平治疗)和低温诱导的细胞减少(用碘甲状腺原氨酸治疗)。此外,本病例提供了从纵向护理中获得的独特见解。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Magnesium and Health Autologous Peripheral Blood Mononuclear Cells can Lead to Pancreatic Beta Cell Regeneration MRI Assessment of Associations between Brown Adipose Tissue and Cachexia in Murine Pancreatic Ductal Adenocarcinoma. Recurrent Spontaneous Jejunal Hematomas Resulting in Bowel Obstruction Multiple Brain Abscesses Caused by Streptococcus intermedius: Prognostic Index of Mortality
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1