先天性脊柱后凸伴1型肌强直性营养不良病例报告:围手术期及麻醉考虑。

IF 0.5 Q3 Medicine Journal of Pediatric Neurosciences Pub Date : 2021-10-01 DOI:10.4103/jpn.JPN_119_20
Arpit Agrawal, Tanvi Dhawale, Varinder Kaur, Gouri Rao Passi
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引用次数: 0

摘要

先天性脊柱后凸合并1型肌强直性营养不良(DM 1)是一种罕见的合并,手术和麻醉干预都具有挑战性。肌肉萎缩症的出现可能加速脊柱侧凸的进展,因此需要手术治疗。本病例报告的目的是讨论这类病例的围手术期麻醉和手术处理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Case Report of Congenital Kyphoscoliosis with Myotonic Dystrophy Type 1: Perioperative and Anesthetic Considerations.

Congenital kyphoscoliosis associated with myotonic dystrophy type 1 (DM 1) is a rare combination and carries challenges of surgical as well as anesthetic intervention. The presence of muscular dystrophy may accelerate progression of scoliosis thus requiring surgical treatment. The objective of this case report was to discuss the perioperative anesthetic and surgical management of such cases.

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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
49
期刊介绍: Journal of Pediatric Neurosciences-JPN (ISSN 1817-1745) is official publication of the Indian Society for Pediatric Neurosurgery. The journal is published semiannually. Bibliographic listings: The journal is indexed with Caspur, DOAJ, EBSCO Publishing’s Electronic Databases, Excerpta Medica / EMBASE, Expanded Academic ASAP, Genamics JournalSeek, Google Scholar, Health & Wellness Research Center, Health Reference Center Academic, Hinari, Index Copernicus, OpenJGate, Scimago Journal Ranking, SCOLOAR, SCOPUS, SIIC databases, Ulrich’s International Periodical Directory
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