Have a symptom?
See what questions
a doctor would ask.

Unverricht-Lundborg syndrome

Unverricht-Lundborg syndrome: Introduction

Unverricht-Lundborg syndrome: A rare inherited type of progressive myoclonus epilepsy which tends to cause symptoms during childhood. The involuntary muscle movements tend to occur more frequently and become more severe with increasing age. Symptoms may occur following various stimuli such as light, stress or exercise. More detailed information about the symptoms, causes, and treatments of Unverricht-Lundborg syndrome is available below.

Symptoms of Unverricht-Lundborg syndrome

Home Diagnostic Testing

Home medical testing related to Unverricht-Lundborg syndrome:

Wrongly Diagnosed with Unverricht-Lundborg syndrome?

Unverricht-Lundborg syndrome: Complications

Review possible medical complications related to Unverricht-Lundborg syndrome:

Causes of Unverricht-Lundborg syndrome

More information about causes of Unverricht-Lundborg syndrome:

Unverricht-Lundborg syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Unverricht-Lundborg syndrome

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see more »

Unverricht-Lundborg syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Unverricht-Lundborg syndrome: Animations

Prognosis for Unverricht-Lundborg syndrome

Prognosis for Unverricht-Lundborg syndrome: The prognosis is quite variable. Some patients have their symptoms stabilize or even improve after a period of progression whereas others continue to have severe symptoms and die prematurely. Patients who respond favorably to treatment may have a normal life expectancy.

Research about Unverricht-Lundborg syndrome

Visit our research pages for current research about Unverricht-Lundborg syndrome treatments.

Clinical Trials for Unverricht-Lundborg syndrome

The US based website lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on for Unverricht-Lundborg syndrome include:

Unverricht-Lundborg syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Unverricht-Lundborg syndrome, or answer someone else's question, on our message boards:

Definitions of Unverricht-Lundborg syndrome:

An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, dysarthria, and intention tremor. Myoclonic seizures are severe and continuous, and tend to be triggered by movement, stress, and sensory stimuli. The age of onset is between 8 and 13 years, and the condition is relatively frequent in the Baltic region, especially Finland. (From Menkes, Textbook of Child Neurology, 5th ed, pp109-110) - (Source - Diseases Database)

Related Unverricht-Lundborg syndrome Info

More information about Unverricht-Lundborg syndrome

  1. Unverricht-Lundborg syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
  8. Prognosis

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise