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Juvenile Myasthenia Gravis – a Limited Case Series and Investigation of Current Guidelines

Author:Kumar, Arjun   Go, Jonathan   Iqbal, Fatiha   Pascuzzi, Robert   Sokol, Deborah   

Session Name:P5: Child Neurology and Developmental Neurology: Neuromuscular 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P5.017  

Author Institution:Indiana University School of Medicine, Indianapolis, IN  

STAC3-related congenital myopathy in a Guarani Mbya patient from southern Brazil - a case report

Author:Ruggiero Comunelo Rodrigues, Gabriela   Tobias Bravo Leite, Martim   Arriaga Criscuoli de Farias, Frederico   Machado Schlindwein, Marco Antônio   Simão Medeiros, Leonardo   Alex Morales Saute, Jonas   Brea Winckler, Pablo   

Session Name:P5: Child Neurology and Developmental Neurology: Neuromuscular 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P5.018  

Author Institution:

Recurrent Lower Extremity Weakness in a Healthy Adolescent Male: A Diagnostic Journey to Hypokalemic Periodic Paralysis Due to SCN4A Mutation

Author:Taskin, Didem   Abram, Harry   

Session Name:P5: Child Neurology and Developmental Neurology: Neuromuscular 1  

Topic:Child Neurology and Developmental Neurology  

Program Number:P5.020  

Author Institution:Mayo Clinic/Nemours Children Clinic/Divison of Neurology, Jacksonville, FL  Nemours Children Clinic/Divison of Neurology, Jacksonville, FL