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...
| Hauptverfasser: | , , , , , , |
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| Format: | Artikel |
| Sprache: | Russian |
| Veröffentlicht: |
IMA-PRESS LLC
2015-10-01
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| Schriftenreihe: | Неврология, нейропсихиатрия, психосоматика |
| Schlagworte: | |
| Online Zugang: | https://nnp.ima-press.net/nnp/article/view/529 |