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A Fatal Outcome of Ludwig's Angina and Necrotizing Fasciitis Following Traditional Tooth Extraction. 传统拔牙后路德维希心绞痛和坏死性筋膜炎的致命结果。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-17 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S488135
Abdullahi Abdiaziz Abukar, Mihret Adane Woldemichael, Elizabeth Vargas Escalante, Brian Agaba, Yanurkis Duranones Rosales
{"title":"A Fatal Outcome of Ludwig's Angina and Necrotizing Fasciitis Following Traditional Tooth Extraction.","authors":"Abdullahi Abdiaziz Abukar, Mihret Adane Woldemichael, Elizabeth Vargas Escalante, Brian Agaba, Yanurkis Duranones Rosales","doi":"10.2147/IMCRJ.S488135","DOIUrl":"10.2147/IMCRJ.S488135","url":null,"abstract":"<p><p>Ludwig's angina is a potentially fatal condition characterized by a rapid onset of cellulitis that bilaterally involves the submandibular, sublingual, and submental spaces. This report describes the case of a 29-year-old female who presented to us with Ludwig's angina following a tooth extraction performed by a traditional healer in Southwestern Uganda. The patient stayed home for over a week before she could seek formal treatment, and this delay led to severe infection and necrotizing fasciitis with extensive tissue necrosis. Despite multiple in-hospital interventions which included incision, drainage, and debridement, the patient succumbed to complications such as secondary lung infection, septicemia, and disseminated intravascular coagulation (DIC). This case report highlights the importance of timely medical intervention, socioeconomic barriers, and antibiotic resistance challenges.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"1029-1035"},"PeriodicalIF":0.7,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11662627/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142877113","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acute Torticollis Reaction Following Metoclopramide Use in a Pediatric Patient: A Comprehensive Case Report and Appraisal of Current Knowledge. 儿科患者使用甲氧氯普胺后的急性斜颈反应：综合病例报告和对当前知识的评价。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-17 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S484955
Mohamed Farah Gabobe Nor, Rayan Mohamed Salah, Mohammed A M Ahmed, Sakariye Abdullahi Hassan, Mohamed Farah Yusuf Mohamud
{"title":"Acute Torticollis Reaction Following Metoclopramide Use in a Pediatric Patient: A Comprehensive Case Report and Appraisal of Current Knowledge.","authors":"Mohamed Farah Gabobe Nor, Rayan Mohamed Salah, Mohammed A M Ahmed, Sakariye Abdullahi Hassan, Mohamed Farah Yusuf Mohamud","doi":"10.2147/IMCRJ.S484955","DOIUrl":"10.2147/IMCRJ.S484955","url":null,"abstract":"<p><p>Dopamine receptor antagonists like metoclopramide are frequently used in a variety of clinical contexts to treat gastrointestinal disorders and control nausea and vomiting. However, it is associated with a high incidence of extrapyramidal side effects (EPS) in children, including dystonic movements and torticollis. This is the instance of a 9-year-old girl who developed abnormal movements of the neck and tongue, along with torticollis, within 48 hours of receiving intravenous metoclopramide for gastroenteritis. The metoclopramide therapy was discontinued, and supportive measures, including diphenhydramine, were initiated, resulting in the resolution of symptoms. This case highlights the importance of recognizing and managing metoclopramide-induced EPS in pediatric patients.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"1037-1040"},"PeriodicalIF":0.7,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663987/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142882009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Partial Detachment of an ILM Inverted Flap After a Successful Closure of a Full-Thickness Traumatic Macular Hole. 成功封闭全层创伤性黄斑裂孔后的ILM倒瓣部分脱离。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-12 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S495427
Abdulaziz A Al Taisan
{"title":"Partial Detachment of an ILM Inverted Flap After a Successful Closure of a Full-Thickness Traumatic Macular Hole.","authors":"Abdulaziz A Al Taisan","doi":"10.2147/IMCRJ.S495427","DOIUrl":"10.2147/IMCRJ.S495427","url":null,"abstract":"<p><strong>Purpose: </strong>To report a case of partial detachment of an inverted internal limiting membrane (ILM) flap following a successful closure of a full-thickness traumatic macular hole.</p><p><strong>Observations: </strong>A 24-year-old male patient presented with a history of a blunt trauma and a full-thickness macular hole. Visual acuity was (20/50) then deteriorated to (20/100) prior to surgery. He underwent pars plana vitrectomy with an inverted ILM flap and gas tamponade. Postoperatively, successful closure of the hole was noted with a visible hinged ILM flap observed over the retina in optical coherence tomography (OCT). Three months later, the patient presented with a complaint of a central floater. Visual acuity was (20/30) and a partially detached ILM flap was noted in the OCT.</p><p><strong>Conclusions and importance: </strong>Inverted ILM flap might detach from the retinal surface after gas resolution and successful closure of a full-thickness macular hole.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"1025-1028"},"PeriodicalIF":0.7,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11648536/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142836586","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary Umbilical Endometriosis (Villar's Nodule): A Case Report. 原发性脐带子宫内膜异位症（Villar's 结节）：病例报告。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-11 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S500922
Ghulam Yahia Baset, Soma Katawazai
{"title":"Primary Umbilical Endometriosis (Villar's Nodule): A Case Report.","authors":"Ghulam Yahia Baset, Soma Katawazai","doi":"10.2147/IMCRJ.S500922","DOIUrl":"10.2147/IMCRJ.S500922","url":null,"abstract":"<p><p>Primary umbilical endometriosis is a rare condition in which there is endometrial glands and stroma in the umbilicus. Primary umbilical endometriosis is also called villar's nodule. This condition is a diagnostic challenge, the pathophysiology of the disease is not well defined and should be considered in all other pathologies of the umbilicus. Surgery is the treatment of choice. Here we present a case of villar's nodule in a 33-years-old multiparous woman that was successfully treated with surgery.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"1021-1023"},"PeriodicalIF":0.7,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11646424/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142828593","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Guillain-Barre Syndrome with Acute Lymphoblastic Leukemia: Case Report. 格林-巴利综合征合并急性淋巴细胞白血病1例报告。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-10 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S496062
Eman R E Almatar, Sondus Alsharidah, Maha Bourusly, Rania Lotfi Ahmed, Mariam Ahmed Alabdulhadi
{"title":"Guillain-Barre Syndrome with Acute Lymphoblastic Leukemia: Case Report.","authors":"Eman R E Almatar, Sondus Alsharidah, Maha Bourusly, Rania Lotfi Ahmed, Mariam Ahmed Alabdulhadi","doi":"10.2147/IMCRJ.S496062","DOIUrl":"10.2147/IMCRJ.S496062","url":null,"abstract":"<p><p>Guillain-Barré syndrome (GBS) is a rare complication in children with acute lymphoblastic leukemia (ALL). This case report explores the presentation and management of GBS in a 16-year-old male with a history of ALL, who developed GBS during maintenance therapy. The patient exhibited progressive symmetrical weakness, sensory loss, and autonomic dysfunction. Diagnostic workup, including nerve conduction studies and lumbar puncture, confirmed the diagnosis of GBS. Differentiating GBS from vincristine-induced neuropathy, a common challenge in this population, was crucial for appropriate management. The patient responded well to intravenous immunoglobulin and supportive care. This case highlights the importance of considering GBS in the differential diagnosis of neurological complications in children with ALL and emphasizes the need for prompt diagnosis and treatment.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"1013-1018"},"PeriodicalIF":0.7,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11864905/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143523356","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Case Report: Implantable Collamer Lens for Keratoconus with Splinter Cataract. 锥形角膜伴分裂性白内障植入性晶状体一例报告。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-08 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S502174
Danya Aldahan, Sara AlHilali
{"title":"Case Report: Implantable Collamer Lens for Keratoconus with Splinter Cataract.","authors":"Danya Aldahan, Sara AlHilali","doi":"10.2147/IMCRJ.S502174","DOIUrl":"10.2147/IMCRJ.S502174","url":null,"abstract":"<p><strong>Background: </strong>Implantable collamer lens (ICL) could be an effective and safe treatment option for patient with keratoconus. The presence of cataract is considered a relative contraindication to the use of ICL. In this case report, we describe the outcomes of ICL implantation in an eye with keratoconus and splinter cortical cataract sparing the visual axis.</p><p><strong>Case report: </strong>Thirty-six-year-old female patient diagnosed with keratoconus was followed in the outpatient department and sought to be independent of glasses in the right eye. Upon examination she was found to have bilateral splinter cortical cataract not involving the visual axis. She had the best spectacle corrected visual acuity of 20/30; she underwent uneventful implantation of ICL in the right eye with an uncorrected visual acuity of 20/30 post-operatively with no progression of the cataract during the follow-up period.</p><p><strong>Conclusion: </strong>The patient achieved a stable uncorrected visual acuity of 20/30 with no cataract progression after 18 months. Splinter cataract remains stable over time, thus it should not be considered as a contraindication for the implantation of ICL in patients with keratoconus.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"1009-1011"},"PeriodicalIF":0.7,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11636243/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142818079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Juvenile Xanthogranuloma Involving the Left Femur: A Case Report and Literature Review. 青少年左股骨黄色肉芽肿1例报告及文献复习。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-07 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S475662
Xiangying Wang, Xiaodan Geng, Hui Zhang, Yun Liu, Zixuan Liu, Changsheng Yang
{"title":"Juvenile Xanthogranuloma Involving the Left Femur: A Case Report and Literature Review.","authors":"Xiangying Wang, Xiaodan Geng, Hui Zhang, Yun Liu, Zixuan Liu, Changsheng Yang","doi":"10.2147/IMCRJ.S475662","DOIUrl":"10.2147/IMCRJ.S475662","url":null,"abstract":"<p><strong>Background: </strong>Juvenile xanthogranuloma is a rare condition, and femoral involvement is even rarer. We report a case of juvenile xanthogranuloma affecting the femur. To the best of our knowledge, this is the first reported case of femoral juvenile xanthogranuloma in China.</p><p><strong>Case presentation: </strong>A 19-year-old boy began experiencing swelling in various parts of his body at the age of 1 year, followed by pain in his left hip. Preoperative pathology and imaging indicated juvenile xanthogranuloma of the left femur, leading to surgical intervention. Postoperatively, the patient experienced significant relief from left hip discomfort.</p><p><strong>Conclusion: </strong>Surgery can be an effective treatment for juvenile xanthogranuloma involving the femur.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"1003-1007"},"PeriodicalIF":0.7,"publicationDate":"2024-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633303/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142813025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical Remission After Therapeutic Apheresis in a Patient Suffering from Long Term Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): A Case Report. 长期肌痛性脑脊髓炎/慢性疲劳综合征（ME/CFS）患者治疗性采血后临床缓解1例报告
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-12-06 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S476044
Harald Burgard
{"title":"Clinical Remission After Therapeutic Apheresis in a Patient Suffering from Long Term Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): A Case Report.","authors":"Harald Burgard","doi":"10.2147/IMCRJ.S476044","DOIUrl":"10.2147/IMCRJ.S476044","url":null,"abstract":"<p><p>Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a debilitating multifactorial illness characterized by profound fatigue persisting for more than six months, post-exertional malaise, cognitive impairments, and a range of systemic symptoms. Until now, no accepted causal treatment regimens have been available; therapeutic options include different approaches, such as alleviation of symptoms and promotion of energy conservation. In this study, we report the case of a 49-year-old female presented to our center suffering from ME/CFS for more than 15 years, characterised by a strong energy loss and neurological and systemic symptoms; previous therapies remained unsuccessful. Therefore, we decided to perform double-filtration apheresis. After comprehensive laboratory evaluation, including investigation of persistent viral infections, the patient was treated eight times with double-filtration apheresis within a period of 2 years, which resulted in a remarkable sustained clinical remission and significant improvement in her quality of life. Therefore, we conclude that double-filtration apheresis could be an effective therapeutic tool for the treatment of ME/CFS.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"997-1002"},"PeriodicalIF":0.7,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11629661/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142806943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Rare Case Report of a Congenital Imperforate Hymen Causing Obstructive Uropathy and Constipation in an 11-Year-Old Girl. 一例罕见的报告先天性处女膜闭锁导致梗阻性尿路病变和便秘在一个11岁的女孩。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-11-28 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S494697
Cecilia Putri Tedyanto, Sianty Dewi, Fransiscus Iman Santoso, Maria Aloysia Praldinya Ere, Kevan Ryvanto Oeylex
{"title":"A Rare Case Report of a Congenital Imperforate Hymen Causing Obstructive Uropathy and Constipation in an 11-Year-Old Girl.","authors":"Cecilia Putri Tedyanto, Sianty Dewi, Fransiscus Iman Santoso, Maria Aloysia Praldinya Ere, Kevan Ryvanto Oeylex","doi":"10.2147/IMCRJ.S494697","DOIUrl":"https://doi.org/10.2147/IMCRJ.S494697","url":null,"abstract":"<p><p>Imperforate hymen is a rare congenital anomaly that can cause mild to severe complications, which leads to an increase in morbidity rates. The incidence is 1:1000, and there was often a delay in diagnosis since the symptoms were not specific until it caused several complications in other organ systems. We reported a case of obstructive uropathy and constipation in an 11-year-old girl who presented with huge hematocolpos due to imperforate hymen. The main symptom was severe lower abdominal pain with a visual analogue scale of 8. This case shows the significance of a physical examination in diagnosing, increasing efficiency in terms of time and cost, and supporting an earlier diagnosis. A corrective hymenectomy, blood drainage, and hymenoplasty were performed as the definitive management. The patient was able to urinate and defecate within seven hours after surgery. The patient also had her period three weeks after surgery.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"985-989"},"PeriodicalIF":0.7,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11610395/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142768789","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Thyroid-Associated Optic Neuropathy: A Case Report of Optic Neuritis Due to Autoimmune Hypothyroidism. 甲状腺相关性视神经病变：自身免疫性甲状腺功能减退所致视神经炎1例报告。
IF 0.7
International Medical Case Reports Journal Pub Date : 2024-11-27 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S493262
Mohamed Farah Osman Hidig, Mohamed Osman Omar Jeele, Bakar Ali Adam, Hassan Muhumed Mohamed, Mohamed Omar Hassan
{"title":"Thyroid-Associated Optic Neuropathy: A Case Report of Optic Neuritis Due to Autoimmune Hypothyroidism.","authors":"Mohamed Farah Osman Hidig, Mohamed Osman Omar Jeele, Bakar Ali Adam, Hassan Muhumed Mohamed, Mohamed Omar Hassan","doi":"10.2147/IMCRJ.S493262","DOIUrl":"https://doi.org/10.2147/IMCRJ.S493262","url":null,"abstract":"<p><strong>Introduction: </strong>Optic neuritis is an uncommon complication of autoimmune hypothyroidism, which is often referred to as thyroid-associated optic neuropathy (TAON).</p><p><strong>Case report: </strong>The case features a 22-year-old Somali woman who had no previous medical conditions. She had sudden vision loss, mainly in her right eye. This was accompanied by joint discomfort, muscular weakness, headaches, and weariness. The clinical examination showed complete absence of light perception in the right eye and there was a relative afferent pupillary deficit, and the thyroid function tests indicated severe hypothyroidism with significantly high levels of thyroid-stimulating hormone (TSH) and low levels of free Triiodothyronine (T3) and Thyroxine (T4). The diagnosis of autoimmune hypothyroidism was confirmed by the presence of positive anti-thyroid peroxidase (anti-TPO) and anti-thyroglobulin antibodies. Treatment was promptly initiated with high-dose corticosteroids (methylprednisolone) and levothyroxine replacement medication. Subsequently, her field of vision and visual acuity, when corrected with the best possible lenses, showed a considerable improvement. Further assessments demonstrated the restoration of normal thyroid function and the complete remission of symptoms related to ocular neuritis, with no further instances of recurrence.</p><p><strong>Conclusion: </strong>The present case emphasizes the crucial need of promptly identifying and handling TAON in order to achieve positive visual results. This highlights the need of taking into account autoimmune hypothyroidism as a potential cause of ocular neuritis. Additional study is necessary to clarify the exact pathophysiological pathways that link autoimmune hypothyroidism to inflammation of the optic nerve, as well as to investigate the most effective therapy strategies.</p>","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"991-995"},"PeriodicalIF":0.7,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11608536/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142768790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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