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"Kyung Eun Nam"

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"Kyung Eun Nam"

Clinical Practice Guideline

Clinical Practice Guidelines for Diagnosis and Non-Surgical Treatment of Primary Frozen Shoulder
Byung Chan Lee, Beom Suk Kim, Byeong-Ju Lee, Chang-Won Moon, Chul-Hyun Park, Dong Hwan Kim, Dong Hwan Yun, Donghwi Park, Doo Young Kim, Du Hwan Kim, Gi-Wook Kim, Hyun Jung Kim, Il-Young Jung, In Jong Kim, Jae Hyeon Park, Jae-Hyun Lee, Jaeki Ahn, Jae-Young Lim, Jin A Yoon, Jong Hwa Lee, Jong-Moon Hwang, Keewon Kim, Kyeong Eun Uhm, Kyoung Hyo Choi, Kyung Eun Nam, Kyunghoon Min, Min Cheol Chang, Myung Woo Park, Nackhwan Kim, Hyeng-Kyu Park, Seong Hun Kim, Seoyon Yang, Sun Jae Won, Sung Gyu Moon, Sung Joon Chung, Sungju Jee, Woo Hyung Lee, Yong Bok Park, Yoonju Na, Yu Hui Won, Yu Jin Im, Yu Sung Yoon, Yun Jung Lee, Yunsoo Soh, Jae-Young Han
Ann Rehabil Med 2025;49(3):113-138.   Published online June 30, 2025
DOI: https://doi.org/10.5535/arm.250057
Objective
Primary frozen shoulder causes significant pain and progressively restricts shoulder movements. Diagnosis is primarily clinically based on patient history and physical examination. Management is mainly non-invasive owing to its self-limiting clinical course. However, clinical practice guidelines for frozen shoulder have not yet been developed in Korea. The developed guidelines aim to provide evidence-based recommendations for the diagnosis and treatment of frozen shoulder.
Methods
A guideline development committee reviewed the literature from four databases (PubMed, Embase, Cochrane Library, and KMbase). Using the PICO (Population, Intervention, Comparator, and Outcome) framework, the committee formulated two backgrounds and 16 key questions to address common clinical concerns. Recommendations were made using the Grading of Recommendations, Assessment, Development, and Evaluation framework.
Results
Diabetes, thyroid disease, and dyslipidemia significantly increase the risk of developing a frozen shoulder. Although frozen shoulder is often self-limiting, some patients may experience long-term disabilities. Ultrasound and magnetic resonance imaging should be used as adjunctive tools alongside clinical diagnosis, and not as independent diagnostic methods. Noninvasive approaches, such as medications, physical modalities, exercises, electrical stimulation, and manual therapy, may reduce pain and improve shoulder function. Other noninvasive interventions have limited evidence, and their application should be based on clinical judgment. Intra-articular steroid injections are recommended for treatment, and physiotherapy or hydrodilatation with steroid injections can also be beneficial.
Conclusion
These guidelines provide evidence-based recommendations for diagnosing and treating primary frozen shoulder.

Citations

Citations to this article as recorded by  
  • Comparison of efficacy of intra-articular injection of platelet-rich plasma with bupivacaine and steroid combination in chronic shoulder pain
    Naveen Malhotra, Neha Sinha, Amit Kumar, Ritu, Disha Gupta, Naman Malhotra
    Journal of Anaesthesiology Clinical Pharmacology.2026; 42(1): 120.     CrossRef
  • 27,347 View
  • 691 Download
  • 1 Web of Science
  • 1 Crossref

Original Article

Effects of Copy Number Variations on Developmental Aspects of Children With Delayed Development
Kee-Boem Park, Kyung Eun Nam, Ah-Ra Cho, Woori Jang, Myungshin Kim, Joo Hyun Park
Ann Rehabil Med 2019;43(2):215-223.   Published online April 30, 2019
DOI: https://doi.org/10.5535/arm.2019.43.2.215
Objective
To determine effects of copy number variations (CNV) on developmental aspects of children suspected of having delayed development.
Methods
A retrospective chart review was done for 65 children who underwent array-comparative genomic hybridization after visiting physical medicine & rehabilitation department of outpatient clinic with delayed development as chief complaints. Children were evaluated with Denver Developmental Screening Test II (DDST-II), Sequenced Language Scale for Infants (SELSI), or Preschool Receptive-Expressive Language Scale (PRES). A Mann-Whitney U test was conducted to determine statistical differences of developmental quotient (DQ), receptive language quotient (RLQ), and expressive language quotient (ELQ) between children with CNV (CNV(+) group, n=16) and children without CNV (CNV(–) group, n=37).
Results
Of these subjects, the average age was 35.1 months (mean age, 35.1±24.2 months). Sixteen (30.2%) patients had copy number variations. In the CNV(+) group, 14 children underwent DDST-II. In the CNV(–) group, 29 children underwent DDSTII. Among variables, gross motor scale was significantly (p=0.038) lower in the CNV(+) group compared with the CNV(–) group. In the CNV(+) group, 5 children underwent either SELSI or PRES. In the CNV(–) group, 27 children underwent above language assessment examination. Both RLQ and ELQ were similar between the two groups.
Conclusion
The gross motor domain in DQ was significantly lower in children with CNV compared to that in children without CNV. This result suggests that additional genetic factors contribute to this variability. Active detection of genomic imbalance could play a vital role when prominent gross motor delay is presented in children with delayed development.

Citations

Citations to this article as recorded by  
  • Novel JAG1 variants leading to Alagille syndrome in two Chinese cases
    Xiufang Feng, Jiangyuan Ping, Shan Gao, Dong Han, Wenxia Song, Xiaoze Li, Yilun Tao, Lihong Wang
    Scientific Reports.2024;[Epub]     CrossRef
  • Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age
    Catherine A. Brownstein, Elise Douard, Robin L. Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan, Bree Martin, Sanda Alexandrescu, Elisabeth A. Haas, Sara O. Vargas, Monica H. Wojcik, Sébastien Jacquemont, Annapurna H. Poduri, Richard D. Goldstei
    Advanced Genetics.2023;[Epub]     CrossRef
  • Copy number variation of the ZNF679 gene in cattle and its association analysis with growth traits
    Xingya Song, Xinmiao Li, Xian Liu, Zijing Zhang, Xiaoting Ding, Yanan Chai, Zhiming Li, Hongli Wang, Jungang Li, Huifeng Liang, Xiaoyan Sun, Guojie Yang, Zengfang Qi, Fuying Chen, Qiaoting Shi, Eryao Wang, Baorui Ru, Chuzhao Lei, Hong Chen, Wujun Liu, Yon
    Animal Biotechnology.2023; 34(9): 4680.     CrossRef
  • Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
    Nadja Louw, Nadia Carstens, Zané Lombard
    Frontiers in Genetics.2023;[Epub]     CrossRef
  • CNV profiles of Chinese pediatric patients with developmental disorders
    Haiming Yuan, Shaofang Shangguan, Zhengchang Li, Jingsi Luo, Jiasun Su, Ruen Yao, Shun Zhang, Chen Liang, Qian Chen, Zhijie Gao, Yanli Zhu, Shujie Zhang, Wei Li, Weiliang Lu, Yu Zhang, Hua Xie, Fang Liu, Qingming Wang, Yangyang Lin, Liying Liu, Xiuming Wa
    Genetics in Medicine.2021; 23(4): 669.     CrossRef
  • Copy Number Variation: Methods and Clinical Applications
    Ondrej Pös, Jan Radvanszky, Jakub Styk, Zuzana Pös, Gergely Buglyó, Michal Kajsik, Jaroslav Budis, Bálint Nagy, Tomas Szemes
    Applied Sciences.2021; 11(2): 819.     CrossRef
  • 9,337 View
  • 115 Download
  • 5 Web of Science
  • 6 Crossref
Case Reports
Botulinum Toxin Type A Injection for Neuropathic Pain in a Patient With a Brain Tumor: A Case Report
Kyung Eun Nam, Joon Sung Kim, Bo Young Hong, Bomi Sul, Hyehoon Choi, So Yeon Jun, Seong Hoon Lim
Ann Rehabil Med 2017;41(6):1088-1092.   Published online December 28, 2017
DOI: https://doi.org/10.5535/arm.2017.41.6.1088

Neuropathic pain is usually managed pharmacologically, rather than with botulinum toxin type A (BTX-A). However, medications commonly fail to relieve pain effectively or have intolerable side effects. We present the case of a 62-year-old man diagnosed with an intracranial chondrosarcoma, which was removed surgically and treated with radiation therapy. He suffered from neuropathic pain despite combined pharmacological therapy with gabapentin, amitriptyline, tramadol, diazepam, and duloxetine because of adverse effects. BTX-A (100 units) was injected subcutaneously in the most painful area in the posterior left thigh. Immediately after the injection, his pain decreased significantly from 6/10 to 2/10 on a visual analogue scale. Pain relief lasted for 12 weeks. This case report describes intractable neuropathic pain caused by a brain tumor that was treated with subcutaneous BTX-A, which is a useful addition for the management of neuropathic pain related to a brain tumor.

Citations

Citations to this article as recorded by  
  • The Esthetic Use of Botulinum Toxins in Cancer Patients: Providing a Foundation for Future Indications
    Marco Papagni, Monica Renga, Selene Mogavero, Paolo Veronesi, Maurizio Cavallini
    Toxins.2025; 17(1): 31.     CrossRef
  • A Systematic Review of Non-Opioid Pain Management in Chiari Malformation (Type 1) Patients: Current Evidence and Novel Therapeutic Opportunities
    Awinita Barpujari, Alina Kiley, Jennifer A. Ross, Erol Veznedaroglu
    Journal of Clinical Medicine.2023; 12(9): 3064.     CrossRef
  • Botulinum Toxin Treatment for Cancer-Related Disorders: A Systematic Review
    Delaram Safarpour, Bahman Jabbari
    Toxins.2023; 15(12): 689.     CrossRef
  • Botulinum Neurotoxins and Cancer—A Review of the Literature
    Shivam O. Mittal, Bahman Jabbari
    Toxins.2020; 12(1): 32.     CrossRef
  • Ocular Neuropathic Pain: An Overview Focusing on Ocular Surface Pains


    Nazanin Ebrahimiadib, Fardin Yousefshahi, Parisa Abdi, Mohammadreza Ghahari, Bobeck S Modjtahedi
    Clinical Ophthalmology.2020; Volume 14: 2843.     CrossRef
  • 6,951 View
  • 64 Download
  • 6 Web of Science
  • 5 Crossref
Progressive Bilateral Facial Palsy as a Manifestation of Granulomatosis With Polyangiitis: A Case Report
Sang Mee Jeong, Joo Hyun Park, Jong In Lee, Kyung Eun Nam, Jung Soo Lee, Joo Hee Kim
Ann Rehabil Med 2016;40(4):734-740.   Published online August 24, 2016
DOI: https://doi.org/10.5535/arm.2016.40.4.734

Bilateral facial palsy, which is usually combined with other diseases, occurs infrequently. It may imply a life-threatening condition. Therefore, the differential diagnosis of bilateral facial palsy is important. However, the etiology is variable, which makes diagnosis challenging. We report a rare case of progressive bilateral facial palsy as a manifestation of granulomatosis with polyangiitis (GPA). A 40-year-old male with otitis media and right facial palsy was referred for electroneurography (ENoG), which showed a 7.7% ENoG. Left facial palsy occurred after 2 weeks, and multiple cavitary opacities were noted on chest images. GPA was diagnosed by lung biopsy. His symptoms deteriorated and mononeuropathy multiplex developed. The possibility of systemic disease, such as GPA, should be considered in patients presenting with bilateral facial palsy, the differential diagnosis of which is summarized in this report.

Citations

Citations to this article as recorded by  
  • Progressive Cranial Nerve Deficits in Granulomatosis With Polyangiitis: A Case Report
    Ryan Waggoner, Imran Bitar, Manasa Pavuloori, Atheel Yako, Natasha Kizy
    Cureus.2025;[Epub]     CrossRef
  • Granulomatosis with polyangiitis presenting as isolated ear involvement: a case series and literature review
    Silvia Zorzi, Gabriele Testa, Michele Tomasoni, Stefano Taboni, Nader Nassif, Gina Alessandra Gregorini, Tommaso Sorrentino, Cesare Piazza, Luca Oscar Redaelli de Zinis
    Acta Otorhinolaryngologica Italica.2025; 45(3): 217.     CrossRef
  • Granulomatosis With Polyangiitis Presenting as Acute Bilateral Facial Nerve Paralysis
    Nicholas Toomey, Aaron J. Done, Doron Sagiv
    Annals of Otology, Rhinology & Laryngology.2025;[Epub]     CrossRef
  • Chameleons, red herrings, and false localizing signs in neurocritical care
    Boyi Li, Tolga Sursal, Christian Bowers, Chad Cole, Chirag Gandhi, Meic Schmidt, Stephan Mayer, Fawaz Al-Mufti
    British Journal of Neurosurgery.2022; 36(3): 298.     CrossRef
  • Bilateral facial nerve palsy responded to immunosuppressive therapy in a patient with eosinophilic granulomatosis with polyangiitis
    Ai Yorishima, Yusuke Yoshida, Yuta Nanao, Naoya Oka, Sho Masuda, Tomohiro Sugimoto, Shintaro Hirata
    Rheumatology Advances in Practice.2022;[Epub]     CrossRef
  • Granulomatosis with polyangiitis presenting with unilateral facial nerve palsy and nasal septum perforation
    Bandar Zaeri, Soha Khan, Asmaa Hegazy, Nayef Al Ghanim
    BMJ Case Reports.2021; 14(1): e236469.     CrossRef
  • Facial Palsy, Radiographic and Other Workup Negative
    Jacqueline J. Greene, Reza Sadjadi, Nate Jowett, Tessa Hadlock
    Neurology Clinical Practice.2021;[Epub]     CrossRef
  • Facial Palsy: A Retrospective Study of 416 Cases Based on Electrodiagnostic Consultation
    Vanessa F.M. Ferreira, Carla R. Graça, João A. Kouyoumdjian
    The Open Neurology Journal.2020; 14(1): 15.     CrossRef
  • Two Different Cases of Simultaneous Bilateral Facial Palsy
    Yeong Jun Park, Tae Kyung Suh, Shin Hye Kim, Moo Jin Baek
    Journal of Clinical Otolaryngology Head and Neck Surgery.2020; 31(2): 188.     CrossRef
  • Look granulomatosis with polyangiitis (GPA) straight in the face: missed opportunities leading to a delayed diagnosis
    N. Rolle, M. Muruganandam, I. Jan, F. M. Harji, J. Harrington, K. N. Konstantinov
    Autoimmunity Highlights.2019;[Epub]     CrossRef
  • 11,543 View
  • 79 Download
  • 6 Web of Science
  • 10 Crossref
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