A Pediatric Case of Sensory Predominant Guillain-Barré Syndrome Following COVID-19 Vaccination [0.03%]
新型冠状病毒疫苗接种后出现的感觉性优势型吉兰-巴雷综合征儿科病例报告
Yunsung Kim,Zahra Zhu,Puneet Kochar et al.
Yunsung Kim et al.
Over six billion doses of Coronavirus Disease 2019 (COVID-19) vaccines have been administered worldwide. Amidst the global COVID-19 vaccination campaign, vaccine-related side effects are of ongoing concern and investigation. According to th...
Acute Cerebellar Ataxia Associated with COVID-19 Infection in a 5-Year-Old Boy [0.03%]
一名5岁男孩感染COVID-19相关的急性小脑共济失调病例报告
Kimberly A O&#x;Neill,Aparna Polavarapu
Kimberly A O&#x;Neill
Background:Neurologic manifestations can occur in many adult patients with COVID-19 but are less frequently described in the literature than the respiratory or inflammatory effects of the disease. There are even fewer reports of the neurolo...
Ahmed Razeq,Samiya Ahmad
Ahmed Razeq
Duchene muscular dystrophy (DMD) is the most common muscular dystrophy in childhood, affecting ∼1:5000 male live births worldwide. DMD is a genetic disorder with X-linked recessive inheritance pattern characterized by a severe muscular phe...
Orthostatic Headaches Associated With Spontaneous Intracranial Hypotension and Autonomic Dysfunction-A Case Series in Young Patients [0.03%]
与低颅压和自主神经功能障碍相关的直立性头痛-年轻患者的系列病例研究
Ankita Ghosh,Yen X Tran,Leon Grant et al.
Ankita Ghosh et al.
Background: Orthostatic headaches can be noted in spontaneous intracranial hypotension and orthostatic intolerance. We present a case series of young patients diagnosed with spontaneous intracranial hypotension and were treated for the same...
Utility and Safety of Perampanel in Pediatric FIRES and Other Drug-Resistant Epilepsies [0.03%]
佩瑞姆帕 nel 在儿科 FIRES 和其他药物难治性癫痫中的有效性和安全性
Guo Yong Lim,Chun Liang Chen,Derrick Chan Wei Shih
Guo Yong Lim
Perampanel is a novel antiepileptic drug, which antagonises AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) glutamate receptor. We describe perampanel as an adjunctive treatment for FIRES (febrile infection-related epilepsy ...
Rhabdomyosarcoma in a Patient With Duchenne Muscular Dystrophy: A Possible Association [0.03%]
杜氏肌营养不良患者出现的横纹肌肉瘤：可能的相关性
Erika Chandler,Lauren Rawson,Robert Debski et al.
Erika Chandler et al.
Duchenne muscular dystrophy (DMD), caused by a mutation in the DMD gene, is known to be associated with co-morbidities including cardiomyopathy, respiratory failure, neuromuscular scoliosis and intellectual disability. Animal studies have e...
Carlos M Guerrero,Sonal Bhatia
Carlos M Guerrero
Primary headache associated with sexual activity (PHASA) is a rare headache syndrome characterized by an acute, maximally intense headache during sexual activity and/or orgasm. While rare, it is a diagnosis that is widely accepted in adults...
Neurophysiological Characteristics of Allgrove (Triple A) Syndrome: Case Report and Literature Review [0.03%]
Allgrove(三A)综合征的神经生理特征：病例报告及文献回顾
Daniel I Weiman,Meredith K Gillespie,Taila Hartley et al.
Daniel I Weiman et al.
Allgrove or "Triple A" syndrome is characterized by alacrima, achalasia, and adrenocorticotropic hormone-resistant adrenal insufficiency, as well as central and peripheral nervous system involvement. Patients demonstrate heterogeneity with ...
Pitt Hopkins-Like Syndrome 1 with Novel CNTNAP2 Mutation in Siblings [0.03%]
具有新型CNTNAP2突变的兄妹中的Pitt-Hopkins样综合症1
Rea Mittal,Ashutosh Kumar,Roger Ladda et al.
Rea Mittal et al.
Pitt Hopkins-like syndrome 1 (PTHLS1, OMIM # 610042) is an ultra-rare autosomal recessive condition with a prevalence of
Jelena De Vrieze,Ingrid M B H van de Laar,Johanneke F de Rijk-van Andel et al.
Jelena De Vrieze et al.
Neurologic disorders caused by mutations in the ATP1A3 gene were originally reported as three distinct rare clinical syndromes: Alternating Hemiplegia of Childhood (AHC), Rapid-onset Dystonia Parkinsonism (RDP) and Cerebellar ataxia, Arefle...