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The Last Revelation
Assessment of EPM2A Gene Mutation Genetics in patients with Epilepsy seizure disorder

Anglais, Allemand · Livre de poche

Expédition généralement dans un délai de 4 à 7 jours ouvrés

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Today, nervous disorders of the nervous system caused by gene changes. Many neurological diseases are of genetic origin. Epilepsy is also the origin of genetic mutations caused by genetic mutations, especially EPM2A is created. In this book we focus on genetic mutations induce a neurological disorder epilepsy. And we analyzed the gene EPM2A. This gene as a major factor in neurological disorder epilepsy plays a role. It also epigenetic factors involved in inducing neurological disorder epilepsy.temporary and transient is caused by cerebral diagnosis of recurrent seizure etiology: idiopathic, stroke, abnormal blood vessels, causes congenital, brain trauma, brain tumors and degenerative diseases of the brain in patients with epilepsy treatment methods new treatment for epilepsy, in addition to drug treatments follow a correct diet and proper nutrition in patients with epilepsy and attention to proper eating habits and adopt a healthier approach to life can help effectively used to control seizures in patients with epilepsy is. Only one type of diet known as the ketogenic diet as a diet rich in fats and non-starchy special and sugar.

A propos de l'auteur










Shahin Asadi,student of Molecular Genetics,Studied Molecular Biology at Tabriz Islamic Azad University Sciences.Bachelor Molecular and Cellular Biology-Genetics,Master of Molecular Biology and Genetics Director of Research,Nuclear Molecular Cell Biology-Genetics Researcher of the National Center for Genetic Engineering and Biotechnology in Iran.


Détails du produit

Auteurs Shahin Asadi
Edition Scholar's Press
 
Contenu Livre
Forme du produit Livre de poche
Date de parution 06.10.2016
Catégorie Sciences naturelles, médecine, it, technique > Biologie > Génétique
 
EAN 9783659843037
ISBN 978-3-659-84303-7
Nombre de pages 636
Dimensions (emballage) 15 x 22 cm
 

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