دورية أكاديمية

Glucose Transporter 1 deficiency and associated conditions in children

التفاصيل البيبلوغرافية
العنوان: Glucose Transporter 1 deficiency and associated conditions in children
المؤلفون: R. G. Gamirova, Z. Afawi, R. R. Gamirova, E. A. Gorobets, V. F. Prusakov, S. Ya. Volgina
المصدر: Rossijskij Vestnik Perinatologii i Pediatrii, Vol 64, Iss 5, Pp 155-158 (2019)
بيانات النشر: Ltd. “The National Academy of Pediatric Science and Innovation”, 2019.
سنة النشر: 2019
المجموعة: LCC:Pediatrics
مصطلحات موضوعية: дети, дефицит транспортера глюкозы i типа, glut1, ген slc2a1, эпилепсия, когнитивные нарушения, кетогенная диета, Pediatrics, RJ1-570
الوصف: The article reviews literature devoted to the glucose transporter type I deficiency syndrome (synonyms: GLUT1 deficiency syndrome, de Vivo disease), that is a genetically determined disease caused by pathogenic variants of the SLC2A1 gene. The insufficiency of this protein leads to the disruption of glucose delivery to the brain through the blood-brain barrier. Clinically, the syndrome is manifested by epileptic seizures (mainly as absences or myoclonic seizures), various motor disorders and psychomotor retardation starting from the early age.Early diagnosis (including molecular genetic analysis of the SLC2A1 gene) enables us to start treatment and prevent progression of the symptoms, and to provide the family with genetic consultation on the prognosis and risks for the next generations. Ketogenic diet is an effective treatment option for this pathological condition, it can lead to a regression of the clinical manifestations, especially on the early stage.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: Russian
تدمد: 1027-4065
2500-2228
Relation: https://www.ped-perinatology.ru/jour/article/view/984; https://doaj.org/toc/1027-4065; https://doaj.org/toc/2500-2228
DOI: 10.21508/1027-4065-2019-64-5-155-158
URL الوصول: https://doaj.org/article/6d09f09de6ae4841bf0038a4f4b36f4f
رقم الأكسشن: edsdoj.6d09f09de6ae4841bf0038a4f4b36f4f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10274065
25002228
DOI:10.21508/1027-4065-2019-64-5-155-158