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When to Question Cerebral Palsy: Hereditary Spastic Paraplegia Masquerading as Cerebral Palsy

Author:Nagabushan, Swathi   Landman, Avi   

Session Name:P4: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:Child Neurology and Developmental Neurology  

Author Institution:UCF/HCA Osceola Hospital, Kissimmee, FL  UCF/HCA Osceola Hospital, Orlando, FL  

Atypical Episodic Hypotonia Responsive to Verapamil in a Child with RYR1 and GNAS Variants

Author:Beltran, Leslie   Cheong, Prescott   Ryan, Casey   Cardona, Carla   Hull, Mariam   

Session Name:P4: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:Child Neurology and Developmental Neurology  

Author Institution:Baylor College of Medicine, Houston, TX  Baylor College of Medicine, Pearland, TX  Texas Children's Hospital, Pediatric Neurology, Houston, TX  

Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay (CLIFAHDD) Syndrome: Case Series and Systematic Review

Author:Garcia Velazquez, Sandra Azareli   Parra Díaz, Paloma   Altintas, Burak   Hadouri, Nawale   Durham, Emily   Martin, Shayanne   Monteil, Arnaud   Gooch, Catherine   Gil-Nagel, Antonio   Calame, Daniel   Tanner, Jeremy   

Session Name:P4: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:Child Neurology and Developmental Neurology  

Author Institution:University of Texas Health Science Center San Antonio, San Antonio, TX  Hospital Universitario Ramón y Cajal, Hospital Ruber Internacional, Fundación Iniciativa para las Neurociencias (FINCE), Spain  Washington University in St. Louis, MO  Dijon-Bourgogne University Hospital, France  Channeling Hope Foundation, TX  Institute of Functional Genomics, University of Montpellier, CNRS, Inserm, France  Hospital Ruber Internacional, Madrid, Spain  Baylor College of Medicine, Child Neurology, Houston, TX  

Metabolic Dysfunction in Shashi-Pena Syndrome: A Novel Pathologic ASXL2 Frameshift Variant

Author:Khoury, Sharbel   Singh, Divya   Jamal, Ali   

Session Name:P4: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:Child Neurology and Developmental Neurology  

Author Institution:Saint Louis University School of Medicine, Saint Louis, MO  SSM Health Cardinal Glennon Children's Hospital-St. Louis University, St Louis, MO  SSM Health Cardinal Glennon Children's Hospital-St. Louis University, MO  

Two-decade Progression to Severe Cognitive and Motor Disability in Megalencephalic Leukoencephalopathy with Subcortical Cysts

Author:Fernandez, Aaron   Padhy, Arpita   Kunhi Veedu, Hari Prasad   

Session Name:P4: Child Neurology and Developmental Neurology: Neurogenetics 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:Child Neurology and Developmental Neurology  

Author Institution:Kern Medical, Bakersfield, CA  United Neuroscience, Inc, Bakersfield, CA