Management of general anesthesia for a patient with Maroteaux type acromesomelic dysplasia complicated with obstructive sleep apnea syndrome and hereditary myopathy.

Pai-Ching Huang; Ju-Hsin Chang; Mei-Ling Shen; Kuen-Bao Chen

首页> 外文期刊>Journal of anesthesia >Management of general anesthesia for a patient with Maroteaux type acromesomelic dysplasia complicated with obstructive sleep apnea syndrome and hereditary myopathy.

【24h】

Management of general anesthesia for a patient with Maroteaux type acromesomelic dysplasia complicated with obstructive sleep apnea syndrome and hereditary myopathy.

机译：Maroteaux型顶体发育异常并发阻塞性睡眠呼吸暂停综合征和遗传性肌病的患者的全身麻醉管理。

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Oropharynx abnormality may lead to difficult intubation in patients with osteochondrodysplasia [1]. For the very rare disease, acromesomelic dysplasia Maroteaux-type (AMDM), which is one such abnormality, however, there is no report whether special consideration is needed in airway management. AMDM is seldom combined with other significant disease [2]. We report the first case of a patient with AMDM complicated by severe obstructive sleep apnea syndrome (OSAS) and hereditary myopathy undergoing smooth management of general anesthesia for elective L4-S1 laminectomy and discectomy.

机译：口咽部异常可能导致骨软骨发育不良的患者插管困难[1]。对于极少见的疾病-顶体发育异常Maroteaux型（AMDM），就是这种异常之一，但是，尚无关于在气道管理中是否需要特别考虑的报道。 AMDM很少与其他重大疾病合并[2]。我们报告的第一例AMDM患者并发严重阻塞性睡眠呼吸暂停综合症（OSAS）和遗传性肌病，正在接受全身麻醉的平稳处理，以进行选择性L4-S1椎板切除术和椎间盘切除术。

著录项

来源
《Journal of anesthesia》 |2012年第4期|共2页
作者
Pai-Ching Huang; Ju-Hsin Chang; Mei-Ling Shen; Kuen-Bao Chen;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类外科学;
关键词

相似文献

外文文献
中文文献
专利

1. Management of general anesthesia for a patient with Maroteaux type acromesomelic dysplasia complicated with obstructive sleep apnea syndrome and hereditary myopathy. [J] . Pai-Ching Huang, Ju-Hsin Chang, Mei-Ling Shen, Journal of anesthesia . 2012,第4期

机译：Maroteaux型顶体发育异常并发阻塞性睡眠呼吸暂停综合征和遗传性肌病的患者的全身麻醉管理。
2. An Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs [J] . Hossein Moravej, Mozhagn Moghtaderi, Sara Mostafavi Journal of Clinical Research in Pediatric Endocrinology . 2020,第1期

机译：伊朗患者患有Maroteaux型acromesomelic发育不良，显示不涉及远端下肢
3. Acromesomelic dysplasia Maroteaux‐type in patients from Vietnam [J] . Tran Thinh Huy, Cao My Ha, Luong Long Hoang, American journal of medical genetics, Part A . 2019,第8期

机译：来自越南患者的acromesomelic dysplasia maroteaux型
4. A pilot study to compare the cerebral hemodynamics between patients with obstructive sleep apnea syndrome (OSA) and periodic limb movement syndrome (PLMS) during nocturnal sleep with near-infrared spectroscopy (NIRS) [C] . Zhongxing Zhang, Maja Schneider, Marco Laures, Conference on Optical Techniques in Neurosurgery, Neurophotonics, and Optogenetics . 2014

机译：通过近红外光谱（NIRS）比较夜间睡眠期间阻塞性睡眠呼吸暂停综合症（OSA）和周期性肢体运动综合症（PLMS）患者的脑血流动力学的初步研究
5. Sleep Bruxism Related Tooth Wear as a Clinical Marker for Obstructive Sleep Apnea/Hypopnea Syndrome in Children. [D] . Singh, Nischal. 2011

机译：睡眠磨牙症相关的牙齿磨损是儿童阻塞性睡眠呼吸暂停/呼吸不足综合征的临床标志。
6. Changes of aldosterone levels in patients with type 2 diabetes complicated by moderate to severe obstructive sleep apnea–hypopnea syndrome before and after treatment with continuous positive airway pressure [O] . Jie Zhang, Lin Tian, Lixin Guo 2019

机译：持续气道正压治疗前后合并中度至重度阻塞性睡眠呼吸暂停低通气综合征的2型糖尿病患者醛固酮水平的变化
7. Changes of aldosterone levels in patients with type 2 diabetes complicated by moderate to severe obstructive sleep apnea–hypopnea syndrome before and after treatment with continuous positive airway pressure [O] . Jie Zhang, Lin Tian, Lixin Guo 2019

机译：2型糖尿病患者的醛固酮水平的变化复杂于中度至重度阻塞呼吸暂停症，在持续正气道压力之前和之后进行治疗前后

Management of general anesthesia for a patient with Maroteaux type acromesomelic dysplasia complicated with obstructive sleep apnea syndrome and hereditary myopathy.

摘要

著录项

相似文献

相关主题

期刊订阅