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Symptoms of Epilepsy

Symptoms of Epilepsy: Introduction

The symptoms, severity, and frequency of epilepsy vary greatly depending on the type of seizure, the cause of the condition, the age and activity level of a person, and other factors.

Many people with epilepsy may experience an aura. An aura is some type of warning that a seizure is approaching. Auras are different in different people, but may include a vague feeing of anxiety or restlessness, visual disturbances, or an unusual sound or odor.

The hallmark symptom of convulsive seizures, also called tonic clonic seizures, in which there is uncontrolled jerking of the body, is not present in all types of epilepsy. Falling, loss of consciousness, and convulsive seizures are typical of grand mal seizures. Symptoms of petit mal seizures are far more subtle and include staring into space, confusion, and being temporarily unresponsive.

During a simple partial seizure, a person does not lose consciousness, but does experience uncontrollable muscle twitching in one area of the body that extends to other areas. During complex partial seizures, a person displays unusual behaviours, such as smacking lips or walking in circles.

Life threatening complications of epilepsy include status epilepticus, in which a seizure lasts more than five minutes or recur frequently. sudden unexplained death in epilepsy can also occur rarely....more about Epilepsy »

Symptoms of Epilepsy

The list of signs and symptoms mentioned in various sources for Epilepsy includes the 31 symptoms listed below:

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Epilepsy: Symptom Checkers

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Epilepsy: Symptom Assessment Questionnaires

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Epilepsy: Complications

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Epilepsy Symptoms: Book Excerpts

Diagnostic Testing

Diagnostic testing of medical conditions related to Epilepsy:

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Do I have Epilepsy?

Epilepsy: Undiagnosed Conditions

Diseases that may be commonly undiagnosed in related medical areas:

Home Diagnostic Testing

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Wrongly Diagnosed with Epilepsy?

The list of other diseases or medical conditions that may be on the differential diagnosis list of alternative diagnoses for Epilepsy includes:

Epilepsy: Research Doctors & Specialists

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Other Possible Causes of these Symptoms

Click on any of the symptoms below to see a full list of other causes including diseases, medical conditions, toxins, drug interactions, or drug side effect causes of that symptom.

Medical Books Online about Epilepsy

Medical Books Excerpts Excerpts of published medical book chapters related to Epilepsy are available from published medical books for more detailed information about Epilepsy.

Medical Books Excerpts
  • Aura
  • "In a Page: Signs and Symptoms" (2004)
  • Chorea
  • "In a Page: Signs and Symptoms" (2004)
  • Chorea
  • "In A Page: Pediatric Signs and Symptoms" (2007)
  • CHOREA
  • "Differential Diagnosis in Primary Care" (2007)
  • MYOCLONUS
  • "Differential Diagnosis in Primary Care" (2007)
  • Aura
  • "Handbook of Signs & Symptoms (Third Edition)" (2006)
  • Myoclonus
  • "Handbook of Signs & Symptoms (Third Edition)" (2006)
  • Seizures
  • "A Pocket Manual of Differential Diagnosis" (1999)
  • Epilepsy
  • "Professional Guide to Diseases (Eighth Edition)" (2005)
  • Aura
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • Myoclonus
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • Seizures
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter" (2000)
  • Seizures
  • "Field Guide to Bedside Diagnosis" (2007)
  • Fasciculations
  • "Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series" (2007)
  • Myoclonus
  • "Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series" (2007)
  • Aura
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Chorea
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Myoclonus
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Seizures
  • "The Diagnostic Approach to Symptoms and Signs in Pediatrics" (2006)
  • Aura
  • "Nursing: Interpreting Signs and Symptoms" (2007)
  • Myoclonus
  • "Nursing: Interpreting Signs and Symptoms" (2007)
  • CHOREA
  • "Differential Diagnosis in Primary Care" (2007)
  • MYOCLONUS
  • "Differential Diagnosis in Primary Care" (2007)
  • Seizures
  • "Pediatric Complaints and Diagnostic Dilemmas" (2003)
 

Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

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Symptoms of Epilepsy: Online Medical Books

16 MEDICAL BOOKS ONLINE! Review excerpts from medical books online, free, without registration, for more information about the symptoms of Epilepsy.


Epilepsy: Signs and symptoms
(Professional Guide to Diseases (Eighth Edition))

The hallmarks of epilepsy are recurring seizures, which can be classified as partial or generalized (some patients may be affected by more than one type).

Partial seizures arise from a localized area of the brain, causing specific symptoms. In some patients, partial seizure activity may spread to the entire brain, causing a generalized seizure. Partial seizures include simple partial (jacksonian) and complex partial seizures (psychomotor or temporal lobe).

A simple partial motor-type seizure begins as a localized motor seizure characterized by a spread of abnormal activity to adjacent areas of the brain. It typically produces stiffening or jerking in one extremity, accompanied by a tingling sensation in the same area. For example, it may start in the thumb and spread to the entire hand and arm. The patient seldom loses consciousness, although the seizure may progress to a generalized seizure.

A simple partial sensory-type seizure involves perceptual distortion, which can include hallucinations.

The symptoms of a complex partial seizure vary but usually include purposeless behavior. The patient experiences an aura immediately before the seizure. An aura represents the beginning of abnormal electrical discharges within a focal area of the brain and may include a pungent smell, GI distress (nausea or indigestion), a rising or sinking feeling in the stomach, a dreamy feeling, an unusual taste, or a visual disturbance. Overt signs of a complex partial seizure include a glassy stare, picking at one’s clothes, aimless wandering, lip-smacking or chewing motions, and unintelligible speech; these signs may last for just a few seconds or as long as 20 minutes. Mental confusion may last several minutes after the seizure; as a result, an observer may mistakenly suspect intoxication with alcohol or drugs or psychosis.

Generalized seizures, as the term suggests, cause a generalized electrical abnormality within the brain and include several distinct types:

❑Absence (petit mal) seizures occur most commonly in children, although they may affect adults as well. They usually begin with a brief change in level of consciousness, indicated by blinking or rolling of the eyes, a blank stare, and slight mouth movements. There’s little or no tonic-clonic movement. The patient retains his posture and continues preseizure activity without difficulty. Typically, each seizure lasts from 1 to 10 seconds. If not properly treated, seizures can recur as often as 100 times per day. An absence seizure may progress to generalized tonic-clonic seizures.

❑A myoclonic (bilateral massive epileptic myoclonus) seizure is characterized by brief, involuntary muscular jerks of the body or extremities, which may occur in a rhythmic fashion and may precede generalized tonic-clonic seizures by months or years.

❑A generalized tonic-clonic (grand mal) seizure typically begins with a loud cry, precipitated by air rushing from the lungs through the vocal cords. The patient then falls to the ground, losing consciousness. The body stiffens (tonic phase) and then alternates between episodes of muscular spasm and relaxation (clonic phase). Tongue-biting, incontinence, labored breathing, apnea, and subsequent cyanosis may also occur. The seizure stops in 2 to 5 minutes, when abnormal electrical conduction of the neurons is completed. The patient then regains consciousness but is somewhat confused and may have difficulty talking. If he can talk, he may complain of drowsiness, fatigue, headache, muscle soreness, and arm or leg weakness. He may fall into deep sleep after the seizure. These seizures may start as facial seizures and spread to become generalized.

An akinetic seizure is characterized by a general loss of postural tone (the patient falls in a flaccid state) and a temporary loss of consciousness. It occurs in young children and is sometimes called a “drop attack” because it causes the child to fall.

Status epilepticus is a continuous seizure state that can occur in all seizure types. The most life-threatening example is generalized tonic-clonic status epilepticus, a continuous generalized tonic-clonic seizure without intervening return of consciousness. Status epilepticus is accompanied by respiratory distress. It can result from abrupt withdrawal of anticonvulsant medications, hypoxic encephalopathy, acute head trauma, metabolic encephalopathy, or septicemia secondary to encephalitis or meningitis.

» READ BOOK EXCERPT ONLINE »

Source: Professional Guide to Diseases (Eighth Edition), 2005

Epilepsy: Signs and symptoms
(Handbook of Diseases)

The hallmark of epilepsy is recurring seizures, which can be classified as partial, generalized, status epilepticus, or unclassified (some patients may be affected by more than one type).

Partial seizures

Arising from a localized area of the brain, partial seizures cause focal symptoms. These seizures are classified by their effect on consciousness and whether they spread throughout the motor strip, causing a generalized seizure. When simple or complex seizures evolve to both sides of the brain, they’re termed secondary generalized seizures.

A simple partial seizure begins locally and generally doesn’t cause an alteration in consciousness. It isn’t uncommon for this type to present with sensory symptoms (lights flashing, smells, hearing hallucinations), autonomic symptoms (sweating, flushing, pupil dilation), and psychic symptoms (dream states, anger, fear). The seizure lasts for a few seconds and occurs without preceding or provoking events.

A complex partial seizure involves impairment in consciousness. Amnesia for the events that occur during and immediately after the seizure is a differentiating characteristic. During the seizure, the patient may follow simple commands. This type of partial seizure generally lasts for 1 to 3 minutes.

Generalized seizures

As the term suggests, generalized seizures cause a generalized electrical abnormality within the brain. They can be convulsive or nonconvulsive and include several types.

Absence seizures occur most commonly in children, although they may affect adults. They usually begin with a brief change in level of consciousness, indicated by blinking or rolling of the eyes, a blank stare, and slight mouth movements. The patient retains his posture and continues preseizure activity without difficulty. Typically, each seizure lasts from 1 to 10 seconds. If not properly treated, seizures can recur as often as 100 times per day. An

absence seizure is a nonconvulsive seizure, but it may progress to a generalized tonic-clonic seizure.

Myoclonic seizures (bilateral massive epileptic myoclonus) are characterized by brief, involuntary muscular jerks of the body or extremities, which may occur in a rhythmic manner. Consciousness isn’t usually affected.

Generalized tonic-clonic seizures typically begin with a loud cry, precipitated by air rushing from the lungs through the vocal cords. The patient then loses consciousness and falls to the ground. The body stiffens (tonic phase) and then alternates between episodes of muscle spasm and relaxation (clonic phase). Tongue biting, incontinence, labored breathing, apnea, and subsequent cyanosis may also occur.

The seizure stops in 2 to 5 minutes, when abnormal electrical conduction of the neurons is completed. The patient then regains consciousness but is confused and may have difficulty talking. If he can talk, he may complain of drowsiness, fatigue, headache, muscle soreness, and arm or leg weakness. He may fall into a deep sleep after the seizure.

Atonic seizures are characterized by a general loss of postural tone and a temporary loss of consciousness. They occur in young children and are sometimes called “drop attacks” because they cause the child to fall.

Status epilepticus

Status epilepticus is a continuous seizure state that can occur in all seizure types. The most life-threatening example is generalized tonic-clonic status epilepticus, a continuous generalized tonic-clonic seizure without intervening return of consciousness.

Status epilepticus is accompanied by respiratory distress. It can result from abrupt withdrawal of anticonvulsant medications, hypoxic encephalopathy, acute head trauma, metabolic encephalopathy, or septicemia secondary to encephalitis or meningitis.

Unclassified seizures

This category is reserved for seizures that don’t fit the characteristics of partial or generalized seizures or status epilepticus. Included as unclassified are events that lack the data to make a more definitive diagnosis.

» READ BOOK EXCERPT ONLINE »

Source: Handbook of Diseases, 2003

Seizures - Case 19-1: 8-Day-Old Girl: IV. Clinical Presentation
(Pediatric Complaints and Diagnostic Dilemmas)

Neonatal L. monocytogenes infection, like group B streptococcal infection, manifests in both an early- and a late-onset form. Clinical manifestations of L. monocytogenes infection are similar to those of other neonatal bacterial infections. Signs of infection include temperature instability, respiratory distress, irritability, lethargy, and poor feeding. In early-onset disease, transplacental transmission after maternal bacteremia or ascending spread from vaginal colonization leads to intrauterine infection with L. monocytogenes. Preterm labor is common among infants with early-onset L. monocytogenes infection; length of gestation is less than 35 weeks in approximately 70% of cases. There is often evidence of an acute febrile maternal illness, with symptoms of fatigue, arthralgias, and myalgias preceding delivery by 2 to 14 days. Blood cultures are positive for L. monocytogenes in 35% of mothers of infants with early-onset listeriosis.
Early-onset infection classically develops within the first or second day of life. Bacteremia (75%) and pneumonia (50%) are usually seen with early-onset infection. Meningitis is seen in 25% of early-onset cases. In severe infection, a granulomatous rash is associated with disseminated disease (granulomatosis infantisepticum). The mortality rate, including stillbirths, is 40% for early-onset infection. In late-onset infection, modes of transmission unrelated to maternal carriage may be involved. Late-onset infection develops during the second to eighth week of life. The most common form of L. monocytogenes infection over this period is meningitis, which is present in approximately 95% of cases. Bacteremia (20%) and pneumonia (10%) are less common. Mortality of late-onset infection is generally low (15%) if the infection is diagnosed early and treated appropriately.
A nosocomial outbreak occurred when nine newborn infants were bathed in mineral oil contaminated with L. monocytogenes. The affected infants developed bacteremia (two cases), meningitis (two cases), or both (five cases); one infant died. Signs of infection developed within 1 week after exposure to the mineral oil.

» READ BOOK EXCERPT ONLINE »

Source: Pediatric Complaints and Diagnostic Dilemmas, 2003

Seizures - Case 19-2: 10-Day-Old Boy: IV. Clinical Presentation
(Pediatric Complaints and Diagnostic Dilemmas)

Signs of hypocalcemia usually develop within the first 3 weeks of life. Signs of neonatal hypocalcemia are often nonspecific and may be seen in a variety of other conditions. Tremors and jitteriness are most commonly seen. Other signs include irritability, hyperreflexia, facial twitching, carpopedal spasm, seizures, cyanosis, and, rarely, laryngospasm. More importantly, other disorders that can manifest with hypocalcemia should be considered. Features of 22q11 deletion syndromes include cleft palate, micrognathia, ear anomalies, bulbous nasal tip, and conotruncal heart defects. Findings associated with Albright hereditary osteodystrophy (pseudohypoparathyroidism type Ia) include round face, short distal phalanges of the thumbs, subcutaneous calcifications, and a family history of developmental delay and dental hypoplasia. Sensorineural deafness, renal dysplasia, and mental retardation are also associated with syndromes that include hypoparathyroidism.

» READ BOOK EXCERPT ONLINE »

Source: Pediatric Complaints and Diagnostic Dilemmas, 2003

Seizures - Case 19-3: 8-Month-Old Boy: IV. Clinical Presentation
(Pediatric Complaints and Diagnostic Dilemmas)

GSD type I is characterized by severe hypoglycemia occurring within 3 to 4 hours after a meal. Although symptomatic hypoglycemia may appear soon after birth, most patients are asymptomatic as long as they receive frequent feeds that contain sufficient glucose to prevent hypoglycemia. Symptoms of hypoglycemia appear only when the interval between feedings increases, such as when the child begins to sleep through the night or when an intercurrent illness disrupts normal feeding patterns.
Patients may have hyperpnea from lactic acidosis. Untreated patients have poor weight gain and growth retardation. Most patients have a protuberant abdomen and hepatomegaly due to glycogen deposition and fatty infiltration. Social and cognitive development are normal unless the infant suffers neurologic impairment after frequent hypoglycemic seizures. Xanthomas may appear on the extensor surfaces of the extremities and buttocks. Older children develop gout.

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Source: Pediatric Complaints and Diagnostic Dilemmas, 2003

Article Excerpts About Symptoms of Epilepsy:

Genes and Disease by the National Center for Biotechnology (Excerpt)

Epilepsy can strike at any time of life --- from infancy to old age. While epilepsy varies widely in type and severity, all forms of this disorder are characterized by recurring seizures resulting from abnormal cell firing in the brain. (Source: Genes and Disease by the National Center for Biotechnology)

NINDS Epilepsy Information Page: NINDS (Excerpt)

Having a seizure does not necessarily mean that a person has epilepsy. Only when a person has had two or more seizures is he or she considered to have epilepsy. (Source: excerpt from NINDS Epilepsy Information Page: NINDS)

Epilepsy as a Cause of Symptoms or Medical Conditions

When considering symptoms of Epilepsy, it is also important to consider Epilepsy as a possible cause of other medical conditions. The Disease Database lists the following medical conditions that Epilepsy may cause:

- (Source - Diseases Database)

Epilepsy as a symptom:

For a more detailed analysis of Epilepsy as a symptom, including causes, drug side effect causes, and drug interaction causes, please see our Symptom Center information for Epilepsy.

Medical articles and books on symptoms:

These general reference articles may be of interest in relation to medical signs and symptoms of disease in general:

About signs and symptoms of Epilepsy:

The symptom information on this page attempts to provide a list of some possible signs and symptoms of Epilepsy. This signs and symptoms information for Epilepsy has been gathered from various sources, may not be fully accurate, and may not be the full list of Epilepsy signs or Epilepsy symptoms. Furthermore, signs and symptoms of Epilepsy may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Epilepsy symptoms.

 
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