Glucose transporter type 1 deficiency syndrome (GLUT1-DS) – delayed diagnosis and treatment. A case report
Authors
Piotr Bogucki
Department of Neurology and Epileptology, Centre of Postgraduate Medical Education, Warsaw, Poland
Ewa Nagańska
Department of Neurology and Epileptology, Centre of Postgraduate Medical Education, Warsaw, Poland
Marta Jurek
Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland
Dorota Hoffman-Zacharska
Department of Neurology and Epileptology, Centre of Postgraduate Medical Education, Warsaw, Poland
Anna Kutkowska-Kaźmierczak
Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland
Ewa Obersztyn
Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland
Urszula Fiszer
Department of Neurology and Epileptology, Centre of Postgraduate Medical Education, Warsaw, Poland
Language: English
Page range: 49 - 54
Submitted on: Oct 3, 2019
Accepted on: Nov 4, 2019
Published on: Nov 21, 2019
Published by: The Foundation of Epileptology
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Related subjects:
© 2019 Piotr Bogucki, Ewa Nagańska, Marta Jurek, Dorota Hoffman-Zacharska, Anna Kutkowska-Kaźmierczak, Ewa Obersztyn, Urszula Fiszer, published by The Foundation of Epileptology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.