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Glucose transporter type 1 deficiency syndrome (GLUT1-DS) – delayed diagnosis and treatment. A case report Cover

Glucose transporter type 1 deficiency syndrome (GLUT1-DS) – delayed diagnosis and treatment. A case report

Open Access
|Nov 2019

Authors

Piotr Bogucki

Department of Neurology and Epileptology, Centre of Postgraduate Medical Education, Warsaw, Poland

Ewa Nagańska

enaganska@yahoo.com

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
DOI: https://doi.org/10.21307/joepi-2019-006 | Journal eISSN: 2299-9728 | Journal ISSN: 2300-0147
Language: English
Page range: 49 - 54
Submitted on: Oct 3, 2019
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Accepted on: Nov 4, 2019
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Published on: Nov 21, 2019
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 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.