Learn About Lambert-Eaton Syndrome

What is the definition of Lambert-Eaton Syndrome?

Lambert-Eaton myasthenic syndrome (LEMS) is a rare disorder in which faulty communication between nerves and muscles leads to muscle weakness.

What are the alternative names for Lambert-Eaton Syndrome?

Myasthenic syndrome; Eaton-Lambert syndrome; Lambert-Eaton syndrome; LES

What are the causes of Lambert-Eaton Syndrome?

LEMS is an autoimmune disorder. This means your immune system mistakenly targets healthy cells and tissues in the body. With LEMS, antibodies produced by the immune system attack nerve cells. This makes nerves cells unable to release enough of a chemical called acetylcholine. This chemical transmits impulses between nerves and muscles. The result is muscle weakness.

LEMS may occur with cancers such as small cell lung cancer or autoimmune disorders such as vitiligo, which leads to a loss of skin pigment.

LEMS affects men more often than women. The most common age of occurrence is around age 60 years. LEMS is rare in children.

What are the symptoms of Lambert-Eaton Syndrome?

Weakness or loss of movement that can be more or less severe, including:

  • Difficulty climbing stairs, walking, or lifting things
  • Muscle pain
  • Drooping of the head
  • The need to use the hands to get up from a sitting or lying position
  • Problems talking
  • Problems chewing or swallowing, which may include gagging or choking
  • Vision changes, such as blurry vision, double vision, and problem keeping a steady gaze

Weakness is generally mild in LEMS. Leg muscles are mostly affected. Weakness may improve after exercise, but continuous exertion causes fatigue in some cases.

Symptoms related to the other parts of the nervous system often occur, and may include:

  • Blood pressure changes
  • Dizziness upon standing
  • Dry mouth
  • Erectile dysfunction
  • Dry eyes
  • Constipation
  • Decreased sweating
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What are the current treatments for Lambert-Eaton Syndrome?

The main goals of treatment are to:

  • Identify and treat any underlying disorders, such as lung cancer
  • Give treatment to help with the weakness

Plasma exchange, or plasmapheresis, is a treatment that helps remove from the body any harmful proteins (antibodies) that are interfering with nerve function. This involves removing blood plasma that contains the antibodies. Other proteins (such as albumin) or donated plasma are then infused into the body.

Another procedure involves using intravenous immunoglobulin (IVIg) to infuse a large amount of helpful antibodies directly into the bloodstream.

Medicines that may also be tried include:

  • Medicines that suppress the immune system's response
  • Anticholinesterase medicines to improve muscle tone (although these are not very effective when given alone)
  • Medicines that increase the release of acetylcholine from nerve cells
Who are the top Lambert-Eaton Syndrome Local Doctors?
David P. Randall
Elite in Lambert-Eaton Syndrome
Elite in Lambert-Eaton Syndrome

Advocate Medical Group Neurology

1875 Dempster St, Ste 625/660, 
Park Ridge, IL 
Languages Spoken:
English

David Randall is a Neurologist in Park Ridge, Illinois. Dr. Randall is rated as an Elite provider by MediFind in the treatment of Lambert-Eaton Syndrome. His top areas of expertise are Lambert-Eaton Syndrome, Peripheral Neuropathy, Chronic Inflammatory Demyelinating Polyneuropathy, and Myasthenia Gravis.

Vern C. Juel
Elite in Lambert-Eaton Syndrome
Elite in Lambert-Eaton Syndrome

Duke Electromyography Laboratory - Clinic 1L

40 Duke Medicine Cir, 
Durham, NC 
Experience:
36+ years
Languages Spoken:
English
Offers Telehealth

Vern Juel is a Neurologist in Durham, North Carolina. Dr. Juel has been practicing medicine for over 36 years and is rated as an Elite provider by MediFind in the treatment of Lambert-Eaton Syndrome. His top areas of expertise are Myasthenia Gravis, Lambert-Eaton Syndrome, Inclusion Body Myositis, Meige Syndrome, and Thymectomy.

 
 
 
 
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Elite in Lambert-Eaton Syndrome
Elite in Lambert-Eaton Syndrome
Medical Engineering Course, 
Nagasaki, JP 

Masakatsu Motomura practices in Nagasaki, Japan. Mr. Motomura is rated as an Elite expert by MediFind in the treatment of Lambert-Eaton Syndrome. His top areas of expertise are Lambert-Eaton Syndrome, Myasthenia Gravis, Paraneoplastic Cerebellar Degeneration, Cerebellar Degeneration, and Thymectomy.

What is the outlook (prognosis) for Lambert-Eaton Syndrome?

Symptoms of LEMS may improve by treating the underlying disease, suppressing the immune system, or removing the antibodies. However, paraneoplastic LEMS may not respond as well to treatment. (Paraneoplastic LEMS symptoms are due to an altered immune system response to a tumor). Death is due to underlying malignancy.

What are the possible complications of Lambert-Eaton Syndrome?

Complications of LEMS may include:

  • Difficulty breathing, including respiratory failure (less common)
  • Difficulty swallowing
  • Infections, such as pneumonia
  • Injuries from falls and problems with coordination
When should I contact a medical professional for Lambert-Eaton Syndrome?

Contact your provider if symptoms of LEMS develop.

What are the latest Lambert-Eaton Syndrome Clinical Trials?
Coordination of Rare Diseases at Sanford

Summary: CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, in...

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Patient Observation With Environmental and Wearable Sensors in Myasthenia Gravis

Summary: This observational study seeks to investigate the underlying processes of myasthenia gravis by employing multimodal monitoring techniques. By integrating digital biomarkers alongside clinical monitoring, we aim to enhance the detection of disease activity and establish correlations between digital measures, clinical scores and various questionnaires including sores on quality of life, sleep qualit...

Who are the sources who wrote this article ?

Published Date: June 13, 2024
Published By: Joseph V. Campellone, MD, Department of Neurology, Cooper Medical School at Rowan University, Camden, NJ. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

What are the references for this article ?

Guptill JT, Sanders DB. Disorders of neuromuscular transmission. In: Jankovic J, Mazziotta JC, Pomeroy SL, Newman NJ, eds. Bradley and Daroff's Neurology in Clinical Practice. 8th ed. Philadelphia, PA: Elsevier; 2022:chap 108.

Kaminski HJ. Disorders of neuromuscular transmission. In: Goldman L, Cooney KA, eds. Goldman-Cecil Medicine. 27th ed. Philadelphia, PA: Elsevier; 2024:chap 390.

Moss HE. Eyelid and facial nerve disorders. In: Liu GT, Volpe NJ, Galetta SL, eds. Liu, Volpe, and Galetta's Neuro-Ophthalmology. 3rd ed. Philadelphia, PA: Elsevier; 2019:chap 14.