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先天性高位气道梗阻综合征的产前诊断:两例报告并文献简要回顾

Prenatal diagnosis of congenital high airway obstruction syndrome: report of two cases and brief review of the literature.

作者信息

Artunc Ulkumen Burcu, Pala Halil Gursoy, Nese Nalan, Tarhan Serdar, Baytur Yesim

机构信息

Celal Bayar University, School of Medicine, Obstetrics and Gynecology Department, Manisa, Turkey.

出版信息

Case Rep Obstet Gynecol. 2013;2013:728974. doi: 10.1155/2013/728974. Epub 2013 Oct 22.

Abstract

Congenital high airway obstruction syndrome (CHAOS) is the obstruction of the fetal upper airways, which may be partial or complete. It is usually incompatible with life. Prenatal recognition of the disease is quite important due to the recently described management options. We report here two cases of CHAOS due to tracheal atresia diagnosed by antenatal ultrasonography and fetal MRI. We also briefly review the relevant literature with the associated management options.

摘要

先天性高气道梗阻综合征(CHAOS)是胎儿上气道的梗阻,可为部分性或完全性。它通常与生命不相容。鉴于最近描述的治疗方案,产前识别该疾病非常重要。我们在此报告两例因气管闭锁导致的CHAOS病例,这些病例通过产前超声和胎儿磁共振成像(MRI)得以诊断。我们还简要回顾了相关文献及相关治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/3819797/22b819912417/CRIM.OBGYN2013-728974.001.jpg

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