DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 05 · Volume 21 · October 2023 DOI: 10.1055/s-013-58371 Pediatric Neuroradiology

Review Article

329
Rana, Abhilasha; Krishnan, Venkatram; Jamwal, Rupie: Spinal Dysraphism Spectrum: A Novel Protocol-based Approach for Accurate Diagnosis on Imaging

Original Article

341
Gowda, Vykuntaraju K.; Channabasappa, Basavakumar; Shivappa, Sanjay K.; Veerappa, Basavaraja G.; Lakshmikantha, Keshavamurthy Mysore: The Clinical, Laboratory, Etiological Profile and Outcome of Acute Necrotizing Encephalitis of Childhood (ANEC) in Tertiary Care Centre from Southern India
347
Cebeci, Hakan; Rykken, Jeffrey; Ott, Frederick; Folkertsma, Mark; Koksel, Yasemin; Gencturk, Mehmet: Microstructural Changes in Normal-Appearing White Matter in Pediatric X-Linked Adrenoleukodystrophy: A Diffusion Tensor Imaging Study
352
Hassanein, Sahar M.A.; Elagouza, Iman; Sakr, Hossam; Mohammed, Maha Z.; Rihan, Ahmed; Deifalla, Shaymaa: Diaphragmatic and Rectus Femoris Muscles Ultrasonography in Relation to Motor and Respiratory Functions in Ambulatory Boys with Duchenne Muscular Dystrophy

Case Report

360
Bastos, Paulo André Dias; Barbosa, Raquel: A Newly Identified Int22h1/Int22h2‐Mediated Xq28 Duplication Syndrome Case Misdiagnosed as Cerebral Palsy
365
Shabo, Leah; Ishaque, Mariam; Sarathy, Danyas; Kumar, Jeyan; Xixis, Kathryn; Park, Min: Pediatric Tacrolimus-Induced Reversible Cerebral Vasoconstriction Syndrome after Heart Transplantation
371
Samur, Bahadir M.; Ercan-Sencicek, Gulhan A.; Gumus, Hakan; Gumus, Gulsum; Baykan, Ali; Caglayan, Ahmet Okay; Per, Huseyin: Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1
377
Das, Suman; Ray, Biman K.; Chakraborty, Uddalak; Kabiraj, Sujoy: A Novel Variant of the Short-Chain Enoyl-CoA Hydratase-1 Gene Presenting with a Mild Phenotype: The Second Case Report from India
384
Freitas, Leonardo F.; Ribeiro, Lays S.; Duarte, Márcio L.; Silva, Mayara O. da; Ferreira, Paula M.: Coffin–Siris Syndrome in a Patient with Hirschsprung's Disease—Expanding the Phenotype by Mutation ARID1B: A Case Report and Literature Review
388
Singh, Kushagra; Lohiya, Sham; Ganvir, Shubhangi; Damke, Sachin: A Case of Acute Necrotizing Encephalitis Following Coronavirus Disease 2019 Infection—A Rare Presentation
391
Jain, Mukesh Kumar; Behera, Chinmaya Kumar; Panda, Sangram; Patnaik, Sibabratta; Sahoo, Bandya; Mishra, Reshmi; Behera, Jyoti Ranjan: A Rare Case of Encephalopathy in Children—Known but Unknown
395
Yadav, Kusumlata; Mishra, Arpita; Narayan, Raghvendra; Singh, Ashok; Agrawal, Ritesh; Mishra, Om Prakash: Homocystinuria Presenting as Ectopia Lentis and Thrombotic Manifestations in Two Siblings: A Case Series
399
Nagabushana, Divya; Samaga, Vishal Vishnuram; Shenoy, Sangeetha; Girishan, Shabari; V. Reddy, Hamsa; AR, Somashekhar: Coronavirus Disease 2019-Associated Cerebral Mucormycosis in an Immunocompetent Child
404
Oyuela-Mancera, Martha E.; Maturana, Jennifer R.; Rodriguez, Laura C.; Perez-Acosta, Juan J.; Rodado-Mieles, César E.; Bastidas, Nicolás: Thalamic Gangliocytoma in a Pediatric Patient—An Incidental Diagnosis

Letter to the Editor

408
Huddar, Akshata; Govindaraj, Periyasamy; Chiplunkar, Shwetha; Nagappa, Madhu; Taly, Arun B.; Sankaran, Bindu Parayil: Paroxysmal Dystonia in a Child with Enoyl-CoA Hydratase Short-Chain 1 (ECHS1) Mutations

Erratum

e1
Samur, Bahadir M.; Ercan-Sencicek, Gulhan A.; Gumus, Hakan; Gumus, Gulsum; Baykan, Ali; Caglayan, Ahmet Okay; Per, Huseyin: Erratum: Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1