Creutzfeldt-Jakob Disease (Case Study)

Authors

  • A.E. Halilova Tashkent Pediatric Medical Institute, Tashkent, Uzbekistan
  • Yo.N. Madjidova Tashkent Pediatric Medical Institute, Tashkent, Uzbekistan

DOI:

https://doi.org/10.61788/njn.v2i15.17

Keywords:

prion disease, Creutzfeldt-Jakob disease

Abstract

The article presents a clinical case of Creutzfeldt-Jakob disease, which is casuistry for our region. This diagnosis after exclusion of all exhibited similar by clinically disease.

References

Неврология. Национальное руководство. Под редакцией Е.И.Гусева, А.Н.Коновалова, В.И.Скворцова, А.Б.Гехт.// -2010.- С. 1017-1028.

Покровский В.И., Киселев О.И., Черкасский Б.Л. Прионы и прионные болезни. - М., 2004. - 384 с.

Prigent S., Rezaer H. PrP assembles // Prion. - 2011. - 5(2). - 68-75.

Ryon C. Prions and prion diseases: Fundamentals and Mechanistic details // J. Microbiol. Biotechnol. - 2007. - №17. -P. 1059-1070.

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Published

10.11.2015

How to Cite

Halilova, A., & Madjidova, Y. (2015). Creutzfeldt-Jakob Disease (Case Study). National Journal of Neurology, 2(8), 114–116. https://doi.org/10.61788/njn.v2i15.17

Issue

2015: No.2 (8) | Special Issue | 80 Anniversary of the Azerbaijan State Advanced Training Institute for Doctors named by A.Aliyev

Section

Clinical Case

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