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Electroretinography Biomarkers Indicate Disrupted Visual Processing in Fragile X Syndrome: A Comparative Study with Healthy Controls

Author:Pu, Qianyi   Sekhar, Tejas   Stanley, Mary   Berry-Kravis, Elizabeth   

Session Name:P2: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P2.015  

Author Institution:Rush Medical College, Chicago, IL  Rush University Medical Center, Chicago, IL  

Case of Autosomal Recessive METTL5 Related Intellectual Disability with Deafness

Author:Daniel, Shreya   Bone, Megan   

Session Name:P2: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P2.016  

Author Institution:Johns Hopkins University School of Medicine, Baltimore, MD  Kennedy Krieger Institute, Baltimore, MD  

Brain Imaging Features in Knobloch Syndrome Type 1 due to COL18A1 Mutation

Author:Garn, Rachel   Gul, Sedat   Anilkumar, Arayamparambil   

Session Name:P2: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P2.017  

Author Institution:College of Medicine, SUNY Upstate Medical University, Syracuse, NY  Department of Neurology, SUNY Upstate Medical University, Syracuse, NY  

Genetic Contributions to Aicardi Syndrome: A Systematic Analysis of Patient Data

Author:Kataria, Sauarbh   Patel, Utsav   Inggas, Made AM   Arya, Prakriti   Karve, Sanidhya S.   Wijaya, Jeremiah H.   

Session Name:P2: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P2.018  

Author Institution:Louisiana State University Health Sciences Center at Shreveport, Shreveport LA 71103, USA, Shreveport, LA  Mayo Clinic, Jacksonville, FL, USA, Jacksonville, FL  

Brain MRI Findings of MVNT-like Lesions in Children with Noonan Syndrome: A Case Series

Author:Rai, Bhavana   van Staalduinen, Eric   Green, Tamar   

Session Name:P2: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P2.019  

Author Institution:Stanford University School of Medicine, Palo Alto, CA  Stanford University School of Medicine, Stanford, CA