Epilepsy: Prevalence, Genetics, and Medication Concerns - Rare Disease

Share to:

Issues related to epilepsy?


Hello, Dr.
Yeh! I am a patient with mild epilepsy.
I used to take medication for over two years, but since I haven't had any seizures afterward, I stopped taking the medication on my own.
I know this is wrong, and I will return for a check-up soon.
However, I have some questions.
What is the prevalence of epilepsy? Since I have it, will my child inherit it from me? If I haven't had any seizures for a while, is it possible that I will never have them again? Thank you, Dr.
Yeh, for your hard work.

tiā, 20~29 year old female. Ask Date: 2005/05/05

Dr. Ye Poxiu reply Rare Disease


Hello: (1) Only a small portion of epilepsy cases are classified as genetically high-risk epilepsy.
Please do not worry.
(2) To determine if it falls under genetically high-risk epilepsy, you can consult your attending physician to discuss the causes of your epilepsy in detail.
(3) Generally speaking, if there have been no seizures for two full years and the EEG is normal, consideration can be given to reducing or even discontinuing medication.
However, it is best to do this under the guidance of a physician to minimize the risk of adverse effects.
(4) In fact, there are no accurate reports on the prevalence of epilepsy in Taiwan.
There is no official data on genetic figures.
PS: I apologize for the delayed response as Dr.
Yeh is currently abroad.
Wishing you well, Dr.
Po-Hsiu Yeh, Department of Neurology, Chi Mei Medical Center.

Reply Date: 2005/05/05

More Info


Hello! Thank you for your thoughtful questions regarding epilepsy, its prevalence, genetics, and medication concerns. It's great to see you taking an active interest in understanding your condition and its implications for your family.


Prevalence of Epilepsy
Epilepsy is one of the most common neurological disorders worldwide. According to the World Health Organization (WHO), approximately 50 million people are affected by epilepsy globally, making it a significant public health concern. In the United States, the prevalence of epilepsy is estimated to be around 1% of the population, which translates to about 3.4 million people. The incidence of epilepsy can vary based on age, with higher rates observed in children and older adults.


Genetics and Hereditary Risks
Regarding your concern about the hereditary nature of epilepsy, it is important to note that while genetics can play a role in the development of epilepsy, it is not solely determined by genetics. Some types of epilepsy have a genetic component, meaning that if a parent has epilepsy, their children may have a higher risk of developing the condition compared to the general population. However, the risk is not absolute. Studies suggest that the risk of developing epilepsy in children of affected parents ranges from 2% to 5%, depending on the specific type of epilepsy and family history.

If you have a specific type of epilepsy that is known to have a genetic basis, it may be beneficial to consult with a genetic counselor. They can provide more detailed information regarding the risks and implications for your children.


Medication and Seizure Control
You mentioned that you had been on medication for over two years and stopped taking it after not experiencing any seizures. While it is common for some individuals with epilepsy to achieve seizure control and eventually discontinue medication, this should always be done under the guidance of a healthcare professional. Stopping medication abruptly can lead to a return of seizures, which can be dangerous.
The decision to stop medication is typically based on several factors, including the duration of seizure freedom, the type of epilepsy, and the individual's overall health. It is crucial to have regular follow-ups with your neurologist to monitor your condition and make informed decisions about your treatment plan.


Future Seizure Activity
As for your concern about whether you will experience seizures again in the future, it is difficult to predict with certainty. Some individuals may remain seizure-free for years after stopping medication, while others may experience a recurrence. Factors such as stress, sleep deprivation, and hormonal changes can trigger seizures in some individuals. Regular check-ups and maintaining a healthy lifestyle can help manage these risks.


Conclusion
In summary, epilepsy is a prevalent neurological condition with a complex interplay of genetic and environmental factors. While there is a hereditary component, the risk of passing it on to your children is relatively low. It is essential to work closely with your healthcare provider regarding medication management and to discuss any concerns about future seizures.
Thank you for your questions, and I wish you the best in your health journey. Please feel free to reach out to your healthcare provider for further clarification or support.

Similar Q&A

Genetic Testing for Epilepsy: Benefits and Treatment Options for Infants

Hello, doctor. I would like to ask how many types of medications are currently available for treating epilepsy in infants? Could you please advise if genetic testing for epilepsy would be helpful in quickly treating the condition? If a specific epilepsy gene is identified, would ...


Dr. Cai Zongzhang reply Neurology
Hello: Epilepsy is currently diagnosed based on clinical symptoms, with genetic testing serving only as a reference, as there is not yet a complete consistency between genotype and clinical phenotype. Medications for infants differ from those for adults, so it is recommended to c...

[Read More] Genetic Testing for Epilepsy: Benefits and Treatment Options for Infants


Managing Epilepsy in Teens: When to Consider Medication and Triggers

Hello, Doctor. My child had their first seizure in the third year of junior high school, characterized by stiffening of the limbs, upward eye movement, and loss of consciousness for about 1-2 minutes (this occurred in March 2015). We went to Chimei Medical Center for an examinati...


Dr. Gao Chunde reply Neurology
It is really difficult to convince oneself and the patient to take medication daily for an event that occurs only once a year. However, if there are indeed structural lesions in the brain, then treatment and medication are necessary. If not, regular follow-up visits are required,...

[Read More] Managing Epilepsy in Teens: When to Consider Medication and Triggers


Managing Dual Antiepileptic Medications: Dosage, Differences, and Side Effects

Hello Dr. Lin, My brother was originally taking the antiepileptic medication Depakene, three times a day at a total of three pills. However, he still occasionally experiences absence seizures and has episodes of generalized tonic-clonic seizures where he loses consciousness and ...


Dr. Lin Zijing reply Neurology
Antiepileptic drugs are intended to prevent the occurrence of seizures, as seizures are caused by abnormal electrical discharges in the brain, which can lead to brain damage, inflammation, atrophy, and even life-threatening situations during severe episodes. Doctors regularly mon...

[Read More] Managing Dual Antiepileptic Medications: Dosage, Differences, and Side Effects


Understanding the Causes of Epilepsy and Tourette Syndrome: A Family Perspective

Hello, my daughter has been taking clonazepam and aripiprazole for a long time. There is no history of epilepsy or Tourette syndrome in our family. Since my daughter is an adult, she is unwilling to discuss her medication. Could you please explain the causes of epilepsy and Toure...


Dr. Huang Xiaoxian reply Psychiatry
Hello Ms. Li: Regarding the medication your daughter is taking, it can be used clinically to treat various different conditions, so it does not necessarily mean that she has epilepsy or Tourette syndrome. From the symptoms you described, it does not seem to align with those condi...

[Read More] Understanding the Causes of Epilepsy and Tourette Syndrome: A Family Perspective


Related FAQ

Epilepsy

(Rare Disease)

Neurology

(Rare Disease)

Tourette Syndrome

(Rare Disease)

Epilepsy

(Neurology)

Rare Disease Treatment

(Rare Disease)

Congenital Metabolic Disorders

(Rare Disease)

Whole Exome Sequencing

(Rare Disease)

Height

(Rare Disease)

G6Pd Deficiency

(Rare Disease)

Hair

(Rare Disease)