The neurological symptoms clinical diagnostics role in patients with genetic diseases

Autor: N. M. Voloshina, D. I. Kebalo, E. D. Zvantseva, M. M. Milica, N. P. Miroshnikova, C. M. Pashchenko
Rok vydání: 2019
Předmět:
Zdroj: Modern medical technology. :69-73
ISSN: 2072-9367
Popis: The purpose of the study. The aim of the publication was to make analysis neurological symptoms peculiarities in patients with the glucose transporter type I deficiency syndrome and to make differential diagnostics with other diseases. There are main clinical symptoms in the patients with glucose transporter type I deficiency syndrome. They include attacks of seizures, movement disorders: paresis, plegia, paroxysmal induced dyskinesias, ballismus, tremor, athetosis, dystonia, ataxia. The glucose transporter type I deficiency syndrome clinical characteristics have been added by the delays of the movement, cognitive development, behavior disorders, head ache. Hardness of the clinical symptoms may fluctuate during a day and depends from the period of eating. The plan for differentiation diagnostics and identification of the neurodegenerative diseases was presented in the article.
Databáze: OpenAIRE