Aggressive Acquired Demyelinating Neuropathy Caused by NF-155: Initially Treatment-Resistant [0.03%]
NF-155所致的进行性加重的获得性脱髓鞘周围神经病对初始治疗无效
Selene Jamall,Nancy Baker,Gordon Peterson et al.
Selene Jamall et al.
Objectives: Anti-neurofascin-155 IgG4 (NF-155) antibody disease has previously been associated with a subset of patients with chronic inflammatory demyelinating polyradiculoneuropathy. We report a case of NF-155 positive ...
Tara Torabi,Adeel S Zubair,Richard J Nowak et al.
Tara Torabi et al.
Thymoma Associated With Autoimmune Encephalitis and Subsequent Myasthenia Gravis [0.03%]
与自身免疫性脑炎和随后发生的重症肌无力相关的胸腺瘤
Syed F Ali,Bridget Nolan,Tyler D&#x;Agostino et al.
Syed F Ali et al.
Otto J Hernandez Fustes
Otto J Hernandez Fustes
Congenital Myasthenic Syndrome Caused by DOK7 Mutation in a Quinquagenarian Male with Calf Hypertrophy [0.03%]
先天性重症肌无力样肌病DOK7突变的五旬老年男性并小腿 hypertrophy 病例报告
Saranya B Gomathy,Animesh Das,Ajay Garg et al.
Saranya B Gomathy et al.
Congenital myasthenic syndromes (CMS) are relatively rare neurologic syndromes of defective neuromuscular transmission that stem from mutations in various proteins at the myoneural junction. Classically, the patients present within the firs...
Juvenile Dermatomyositis Without Skin Lesions in an Antinuclear Matrix Protein 2 Antibody Seropositive Pediatric Case [0.03%]
抗核基质蛋白2抗体阳性儿科患者无皮肤病变的青少年皮肌炎病例报告
Fatma Kamoun,Sirine Laroussi,Azza Mellouli et al.
Fatma Kamoun et al.
We report a 5-year-old boy who presented with progressive weakness in 4 limbs and gait disorders over 7 months. No skin rash was observed on admission. A symmetrical proximodistal weakness was found. The creatine kinase level was normal wit...
Atypical Presentation of Tangier Disease-Expanding the Clinical Spectrum [0.03%]
Tangier病的不典型病例报告-扩展临床谱系
Dipti Baskar,Seena Vengalil,Saraswati Nashi et al.
Dipti Baskar et al.
Tangier disease is an autosomal recessive multisystem metabolic disorder with neuromuscular manifestations including peripheral neuropathy such as multifocal mononeuropathy or pseudosyringomyelia patterns. We report a novel phenotype of Tan...
Tatsuya Oishi,Jennifer Pagano,Cody Sellers et al.
Tatsuya Oishi et al.
Objectives: Periodic paralysis is a rare genetic condition characterized by episodes of neuromuscular weakness, often provoked by electrolyte abnormalities, physiologic stress, physical exertion, and diet. In addition to ...
Mononeuropathy Multiplex After Severe SARS-CoV-2 Infection: A Case Series and Literature Review [0.03%]
严重的SARS-CoV-2感染后单发性多发神经病变的病例系列和文献综述
Alicia E Dupre,Michaël C C Slama
Alicia E Dupre
Introduction: Peripheral nerve injuries are being increasingly recognized in patients recovering from severe SARS-CoV-2 infections. Axonal neuropathies can occur, leading to lasting and disabling deficits. ...
Cytokines Single Nucleotide Polymorphisms (SNPs) Association With Myasthenia Gravis (MG) In Algerian Patients: A Case-Control Study On A Small Group [0.03%]
阿尔及利亚重症肌无力患者细胞因子单核苷酸多态性与重症肌无力的病例对照研究：一组小样本研究
Mohamed Nadji Bouchtout,Fethi Meçabih,Chahrazad Boukadir et al.
Mohamed Nadji Bouchtout et al.
Abstract: Myasthenia gravis (MG) is an autoimmune disease of multifactorial etiology in which genetic factors and cytokines seem to play an important role. The aim of this study was to investigate potential associations o...