Neurofibromatosis and Pregnancy

IF 0.1 Q4 OBSTETRICS & GYNECOLOGY Journal of Clinical Obstetrics and Gynecology Pub Date : 2020-01-01 DOI:10.5336/jcog.2020-78717
R. A. Bilir, İlayda Loçlar Karaalp, A. Karateke
{"title":"Neurofibromatosis and Pregnancy","authors":"R. A. Bilir, İlayda Loçlar Karaalp, A. Karateke","doi":"10.5336/jcog.2020-78717","DOIUrl":null,"url":null,"abstract":"ABS TRACT Neurofibromatosis (NF) is an autosomal dominant genetic syndrome which can be seen in 1: 3000- 1:5000 women. Women with NF without infertility problem may have one or more pregnancies during reproductive years. Pregnancies of patients with neurofibromatosis are known to be complicated by intrauterine growth retardation, preterm birth, gestational hypertension and preeclampsia, but history of abruption is very rare in few cases. Physicians should be aware of the complications of this unique pregnancy and manage it multidisciplinary. The purpose of this case report is to share the experience of the pregnancy with neurofibromatosis, having epilepsy and unexplained em- bolism history, which is complicated with intrauterine growth retardation and placental abruption","PeriodicalId":36268,"journal":{"name":"Journal of Clinical Obstetrics and Gynecology","volume":"1 1","pages":""},"PeriodicalIF":0.1000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Obstetrics and Gynecology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5336/jcog.2020-78717","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

ABS TRACT Neurofibromatosis (NF) is an autosomal dominant genetic syndrome which can be seen in 1: 3000- 1:5000 women. Women with NF without infertility problem may have one or more pregnancies during reproductive years. Pregnancies of patients with neurofibromatosis are known to be complicated by intrauterine growth retardation, preterm birth, gestational hypertension and preeclampsia, but history of abruption is very rare in few cases. Physicians should be aware of the complications of this unique pregnancy and manage it multidisciplinary. The purpose of this case report is to share the experience of the pregnancy with neurofibromatosis, having epilepsy and unexplained em- bolism history, which is complicated with intrauterine growth retardation and placental abruption
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
神经纤维瘤病与妊娠
ABS路神经纤维瘤病(NF)是一种常染色体显性遗传综合征,可在1:30 00- 1:5000的女性中看到。无不育问题的NF患者在生育年龄可能有一次或多次怀孕。神经纤维瘤病患者妊娠合并宫内发育迟缓、早产、妊娠期高血压、先兆子痫,但极少有早剥史。医生应该意识到这种独特的妊娠并发症和管理它的多学科。本病例报告的目的是分享怀孕的经验,神经纤维瘤病,癫痫和不明原因的血栓病史,合并宫内发育迟缓和胎盘早剥
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
Journal of Clinical Obstetrics and Gynecology
Journal of Clinical Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
0.30
自引率
0.00%
发文量
8
期刊最新文献
Management of Congenital Cervical Teratoma with Application of EXIT Protocol - Case Report Reverse Breech Extraction versus Vaginal Push before Uterine Incision during Cesarean Section with Fully Dilated Cervix and Impacted Fetal Head Postdate Pregnancy Maternal and Fetal Outcomes among Sudanese Women Age as a Predictor of Time to Response for Patients Undergoing Medical Management of Endometrial Cancer Ectopic Pregnancy Risk Factors Presentation and Management Outcomes
×
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