Unverricht-Lundborg disease in an adult female patient: A clinical case
Карлов В. А., Жидкова И. А., Мишина Е. Y., Власов П. Н., Маргосюк Н. В., Тингаева Л. П., Перепелова Е. М., Перепелов В. А., Гладов Б. П., Труханов С. А.
Неврология, нейропсихиатрия, психосоматика
Т. 10, С. 56-61
Опубликовано: 2018
Тип ресурса: Статья
DOI:10.14412/2074-2711-2017-1S-56-61
Аннотация:
We have considered it appropriate to publish this case due to the rarity of progressive myoclonus epilepsy; diagnostic difficulties, particularly in the early stages of the disease (the female patient has been long followed up for diagnosed juvenile myoclonic epilepsy); the relative role of a genetic study because it has not brought results in this case, and, finally, a problem with therapy, and a significant contribution to the achievement of certain success of currently available antiepileptic drugs, levetiracetam in particular. © 2018 Ima-Press Publishing House. All rights reserved.
Ключевые слова:
Clinical presentations; Diagnosis; Differential diagnosis; Progressive myoclonus epilepsies; Treatment; Unverricht-Lundborg disease
Язык текста: Русский
ISSN: 2310-1342
Карлов В. А.
Жидкова И. А.
Мишина Е. Y. Е.Ю.
Власов П. Н.
Маргосюк Н. В.
Тингаева Л. П.
Перепелова Е. М. Елена Михайловна 1954-
Перепелов В. А. Всеволод Андреевич 1984-
Гладов Б. П.
Труханов С. А.
Karlov V. A.
Zhidkova I. A.
Mishina E. Y. E.Yu.
Vlasov P. N.
Margosyuk N. V.
Tingaeva L. P.
Perepelova E. M. Elena Mikhaylovna 1954-
Perepelov V. A. Vsevolod Andreevich 1984-
Gladov B. P.
Trukhanov S. A.
Unverricht-Lundborg disease in an adult female patient: A clinical case
Текст визуальный непосредственный
Неврология, нейропсихиатрия, психосоматика
ИМА-Пресс
Т. 10 С. 56-61
2018
Статья
Clinical presentations Diagnosis Differential diagnosis Progressive myoclonus epilepsies Treatment Unverricht-Lundborg disease
We have considered it appropriate to publish this case due to the rarity of progressive myoclonus epilepsy; diagnostic difficulties, particularly in the early stages of the disease (the female patient has been long followed up for diagnosed juvenile myoclonic epilepsy); the relative role of a genetic study because it has not brought results in this case, and, finally, a problem with therapy, and a significant contribution to the achievement of certain success of currently available antiepileptic drugs, levetiracetam in particular. © 2018 Ima-Press Publishing House. All rights reserved.