MARATTO

article · Azhar International Journal of Pharmaceutical and Medical Sciences/Azhar International Journal of Pharmaceutical and Medical Sciences

Gene polymorphism in epilepsy _ review article

Abstract

More than 50 million people globally experience epilepsy, a spectrum of diverse brain illnesses wherein recurrent epileptic seizures are the hallmark. According to International League Against Epilepsy (ILAE) four basic forms of epilepsy are distinguished: focal, generalized, combination generalized and focal, and unknown. Epilepsy may have obvious structural, infectious, metabolic, and immunological etiologies, and its etiology appears to be mostly influenced by genetics, but in the majority of cases, no obvious etiology is found. Early connected studies have identified numerous loci which might include possible genes linked to epilepsy susceptibility, and mutational research have discovered a number of mutations in both ion channel and non-ion channel genes in idiopathic generalized epileptic patients. Such genes may generally cause epilepsy, or they may account only for different types of it. In this article we demonstrated some of these genes and its direct correlation with epilepsy and the specific type idiopathic generalized epilepsy.

Research topics

  • Metabolism and Genetic Disorders
  • Digestive system and related health

Read the original research

This page summarises published work. The authoritative version sits with the publisher.

DOI: 10.21608/aijpms.2024.255876.1247

Is something wrong with this record? Report it or request removal.

Discussion

Discuss this research

Have you built on this work, tried to replicate it, or seen it applied in practice? Share what you know. Verified researchers and MARATTO™ domain experts can open a discussion, and any member can reply. Contributions are reviewed before they appear.

No discussion yet. Open the first thread.