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A Novel Variant of NBEA Causing Paroxysmal Kinesogenic Dyskinesia

Author:Sudheendra, Manasa   Pehlivan, Davut   Lupski, James   Calame, Daniel   Hull, Mariam   

Session Name:P8: Movement Disorders: Rare Movement Disorders  

Topic:Movement Disorders  

Program Number:P8.019  

Author Institution:Texas Children's Hospital/ Baylor College of Medicine, Houston, TX  Baylor College of Medicine, Houston, TX  

A Complex Phenotype in an Adult with Recurrent Syncope

Author:Bansal, Dhruv   Kearney, Seamus   

Session Name:P8: Movement Disorders: Rare Movement Disorders  

Topic:Movement Disorders  

Program Number:P8.020  

Author Institution:Royal Victoria Hospital, Belfast, Belfast, United Kingdom  

Decoding Destiny: The Genetic Puzzle of Adult-onset Alexander Disease

Author:Shrestha, Ramesh   Kara, Sukriye Damla   

Session Name:P8: Movement Disorders: Rare Movement Disorders  

Topic:Movement Disorders  

Program Number:P8.021  

Author Institution:University of Mississippi Medical Center, Jackson, MS  

The Neurological and Hepatic Nexus: Analyzing PFIC3 Presentation as Wilson Disease- Molecular Genetic Diagnosis and Treatment Response

Author:Sondhi, Pulkit   Singh, Jagjot   Kaur, Ramanjot   Kathait, Aparna   Brar, Akrambir Singh   

Session Name:P8: Movement Disorders: Rare Movement Disorders  

Topic:Movement Disorders  

Program Number:P8.022  

Author Institution:BLK-Max Super Speciality Hospital, DELHI, New Delhi, Delhi., India  Government Medical College, Amritsar, Amritsar, India  VMMC & Safdarjung Hospital, New Delhi, New Delhi, Delhi , India  

Illuminating the Presentation of Hereditary Spastic Paraplegia Type 7 (HSP7)

Author:Snyder, Emma   Sanderson, John   Bird, Thomas   Davis, Marie   

Session Name:P8: Movement Disorders: Rare Movement Disorders  

Topic:Movement Disorders  

Program Number:P8.023  

Author Institution:University of Washington Medical Center, Seattle, WA