HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES
The authors provide a review of the clinical and genetic characteristics of hereditary diseases and syndromes accompanied by febrile convulsions, which is illustrated by examples of their own observations. The paper sets forth the possibilities and limitations of using current methods for the molecu...
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| Format: | Article |
| Language: | Russian |
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ABV-press
2016-08-01
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| Series: | Русский журнал детской неврологии |
| Subjects: | |
| Online Access: | https://rjdn.abvpress.ru/jour/article/view/151 |
| _version_ | 1797874451254083584 |
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| author | E. L. Dadali A. A. Sharkov I. V. Sharkova I. V. Kanivets F. A. Konovalov I. A. Akimova |
| author_facet | E. L. Dadali A. A. Sharkov I. V. Sharkova I. V. Kanivets F. A. Konovalov I. A. Akimova |
| author_sort | E. L. Dadali |
| collection | DOAJ |
| description | The authors provide a review of the clinical and genetic characteristics of hereditary diseases and syndromes accompanied by febrile convulsions, which is illustrated by examples of their own observations. The paper sets forth the possibilities and limitations of using current methods for the molecular genetic diagnosis of idiopathic and symptomatic epilepsies. The most effective and less expensive technique of molecular genetic analysis is shown to be an exome sequencing test using the panels of genes responsible for the occurrence of diseases with simi1ar clinical symptoms. The paper also presents the structure of the panel of genes responsible for the occurrence of monogenic epilepsies, which has been designed at the Genomed Clinic and includes 448 genetic variants. It also determines the significance of using a chromosomal microarray analysis to diagnose both chromosomal and monogenic diseases accompanied by convulsions. |
| first_indexed | 2024-04-10T01:32:15Z |
| format | Article |
| id | doaj.art-0bc8a05143dd4211baa8d5a20ac0e9a5 |
| institution | Directory Open Access Journal |
| issn | 2073-8803 2412-9178 |
| language | Russian |
| last_indexed | 2024-04-10T01:32:15Z |
| publishDate | 2016-08-01 |
| publisher | ABV-press |
| record_format | Article |
| series | Русский журнал детской неврологии |
| spelling | doaj.art-0bc8a05143dd4211baa8d5a20ac0e9a52023-03-13T09:30:11ZrusABV-pressРусский журнал детской неврологии2073-88032412-91782016-08-01112334110.17650/2073-8803-2016-11-2-33-41119HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURESE. L. Dadali0A. A. Sharkov1I. V. Sharkova2I. V. Kanivets3F. A. Konovalov4I. A. Akimova5Медико-генетический научный центр, МоскваРоссийский национальный исследовательский медицинский университет им. Н.И. Пирогова. Научно-исследовательский клинический институт педиатрии им. акад. Ю.Е. Вельтищева, МоскваМедико-генетический научный центр, МоскваЛаборатория молекулярной патологии «Геномед», МоскваЛаборатория молекулярной патологии «Геномед», МоскваЛаборатория молекулярной патологии «Геномед», МоскваThe authors provide a review of the clinical and genetic characteristics of hereditary diseases and syndromes accompanied by febrile convulsions, which is illustrated by examples of their own observations. The paper sets forth the possibilities and limitations of using current methods for the molecular genetic diagnosis of idiopathic and symptomatic epilepsies. The most effective and less expensive technique of molecular genetic analysis is shown to be an exome sequencing test using the panels of genes responsible for the occurrence of diseases with simi1ar clinical symptoms. The paper also presents the structure of the panel of genes responsible for the occurrence of monogenic epilepsies, which has been designed at the Genomed Clinic and includes 448 genetic variants. It also determines the significance of using a chromosomal microarray analysis to diagnose both chromosomal and monogenic diseases accompanied by convulsions.https://rjdn.abvpress.ru/jour/article/view/151фебрильные судорогинаследственные синдромыранние эпилептические энцефалопатиигенерализованные эпилепсии с фебрильными судорогами плюсидиопатические эпилепсиисимптоматические эпилепсииэкзомное секвенирование нового поколенияхромосомный микроматричный анализ |
| spellingShingle | E. L. Dadali A. A. Sharkov I. V. Sharkova I. V. Kanivets F. A. Konovalov I. A. Akimova HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES Русский журнал детской неврологии фебрильные судороги наследственные синдромы ранние эпилептические энцефалопатии генерализованные эпилепсии с фебрильными судорогами плюс идиопатические эпилепсии симптоматические эпилепсии экзомное секвенирование нового поколения хромосомный микроматричный анализ |
| title | HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES |
| title_full | HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES |
| title_fullStr | HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES |
| title_full_unstemmed | HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES |
| title_short | HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES |
| title_sort | hereditary diseases and syndromes accompanied by febrile convulsions clinical and genetic characteristics and diagnostic procedures |
| topic | фебрильные судороги наследственные синдромы ранние эпилептические энцефалопатии генерализованные эпилепсии с фебрильными судорогами плюс идиопатические эпилепсии симптоматические эпилепсии экзомное секвенирование нового поколения хромосомный микроматричный анализ |
| url | https://rjdn.abvpress.ru/jour/article/view/151 |
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