The late diagnosis of double cortex syndrome in a 36-year-old woman with resistant atonic seizures

Subcortical laminar heterotopia (double cortex syndrome) is an orphan disease with an incidence of 1 to 200,000 people in the population. The cause of the disease is mutation of the gene DCX (synonyms: DBCN, XLIS) in chromosome Xq22.3-q23. The type of inheritance is X-linked dominant. Correct diagno...

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Hlavní autoři: N. A. Shnayder, D. V. Dmitrenko, Yu. B. Govorina, E. A. Kantimirova, O. V. Alekseeva, A. A. Molgachev, A. A. Makarkin
Médium: Článek
Jazyk:Russian
Vydáno: IMA-PRESS LLC 2015-10-01
Edice:Неврология, нейропсихиатрия, психосоматика
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On-line přístup:https://nnp.ima-press.net/nnp/article/view/529