The neurological symptoms clinical diagnostics role in patients with genetic diseases

Authors

  • M. A. Trishchynskaya Shupyk National Medical Academy of postgraduate education Kyiv, Ukraine, Ukraine
  • V. A. Svystilnyk Shupyk National Medical Academy of postgraduate education Kyiv, Ukraine, Ukraine

DOI:

https://doi.org/10.34287/MMT.2(41).2019.42

Abstract

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.

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Published

2019-08-20

How to Cite

Trishchynskaya, M. A. ., & Svystilnyk, V. A. . (2019). The neurological symptoms clinical diagnostics role in patients with genetic diseases. Modern Medical Technology, (2), 69–73. https://doi.org/10.34287/MMT.2(41).2019.42

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Reviews of literature