LAFORA DISEASE. A DIFFICULT PATIENT IN THE NEUROLOGIST’S PRACTICE
We described a clinical case of Lafora disease, a rare genetically determined disease (mutations in the EPM2Aor EPM2Bgenes) from the group of progressive myoclonus-epilepsy forms with an autosomal recessive type of inheritance. The symptoms of the beginning of Laphora disease are similar to the symp...
| Main Authors: | , |
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| Format: | Article |
| Language: | Russian |
| Published: |
Ltd. “The National Academy of Pediatric Science and Innovation”
2018-11-01
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| Series: | Rossijskij Vestnik Perinatologii i Pediatrii |
| Subjects: | |
| Online Access: | https://www.ped-perinatology.ru/jour/article/view/746 |