对患有赖氨酰羟化酶-3 缺乏症的儿童脊柱侧凸的治疗:病例报告。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Mirbahador Athari, Ardeshir Tajbakhsh, Ahmadreza Mirbolook, Maryamsadat Beheshtian, Mobin Forghan, Dariush Abtahi
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引用次数: 0

摘要

背景:一例罕见的赖氨酰羟化酶缺乏症脊柱侧弯手术病例:一例罕见的赖氨酰羟化酶缺乏症患者接受脊柱侧弯手术的病例报告:一名已知患有赖氨酰羟化酶缺乏症的 8 岁波斯病人因脊柱侧弯而就诊。体格检查时,他面部毛发稀疏,肘关节屈曲挛缩,膝关节屈曲挛缩。他有眼科手术史、马蹄内翻足和听力问题。他接受了脊柱侧弯手术,植入了生长棒器械:结论:这些患者可以谨慎进行手术,外科医生和麻醉师应注意术中和术后可能出现的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of scoliosis in a pediatric patient with lysyl hydroxylase-3 deficiency: a case report.

Background: A rare case report of lysyl hydroxylases deficiency undergoing scoliosis surgery.

Case presentation: An 8-year-old Persian patient with a known case of lysyl hydroxylases deficiency presented with scoliosis. On physical examination, he had course facial hair, elbow flexion contracture, and knee flexion contracture. He had a history of eye surgery, clubfoot, and hearing problems. He underwent scoliosis surgery with growing rod instrumentation.

Conclusion: Surgery can be done in these patients with caution, and the surgeon and anesthesiologist should be aware of potential complications during and after surgery.

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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