Meige's syndrome

Not to be confused with Meigs syndrome.
Not to be confused with Meige disease.
Meige's syndrome
This 16th century painting by Flemish artist Pieter Bruegel is one of the oldest known depictions of the facial tic associated with this syndrome.
Classification and external resources
Specialty neurology
ICD-10 G24.4
ICD-9-CM 333.82
DiseasesDB 31428
MeSH D008538

Meige's syndrome is a type of dystonia. It is also known as Brueghel's syndrome and oral facial dystonia. It is actually a combination of two forms of dystonia, blepharospasm and oromandibular dystonia (OMD).

When OMD is combined with blepharospasm, it may be referred to as Meige’s Syndrome named after Henri Meige,[1] the French neurologist who first described the symptoms in detail in 1910. The symptoms usually begin between the ages of 30 and 70 years old and appear to be more common in women than in men (2:1 ratio). The combination of upper and lower dystonia is sometimes called cranial-cervical dystonia.[2] The incidence is about one case in 20,000 people.[3]


Oromandibular Symptoms

Blepharospasm symptoms

In addition, in some patients, the dystonic spasms may sometimes be provoked by certain activities, such as talking, chewing, or biting. Particular activities or sensory tricks may sometimes temporarily alleviate OMD symptoms, including chewing gum, talking, placing a toothpick in the mouth, lightly touching the lips or chin, or applying pressure beneath the chin.

A few upper and lower dystonia types

Blepharo means "eyelid". Spasm means "uncontrolled muscle contraction". The term blepharospasm ['blef-a-ro-spaz-m] can be applied to any abnormal blinking or eyelid tic or twitch resulting from any cause, ranging from dry eyes to Tourette's syndrome to tardive dyskinesia. The blepharospasm referred to here is officially called benign essential blepharospasm (BEB) to distinguish it from the less serious secondary blinking disorders. "Benign" indicates the condition is not life-threatening, and "essential" is a medical term meaning "of unknown cause". It is both a cranial and a focal dystonia. Cranial refers to the head and focal indicates confinement to one part. The word dystonia describes abnormal involuntary sustained muscle contractions and spasms. Patients with blepharospasm have normal eyes. The visual disturbance is due solely to the forced closure of the eyelids.

Oromandibular dystonia (OMD) is a form of focal dystonia that affects varying areas of the head and neck including the lower face, jaw, tongue and larynx. The spasms may cause the mouth to pull open, shut tight, or move repetitively. Speech and swallowing may be distorted. It is often associated with dystonia of the cervical muscles (Spasmodic Torticollis), eyelids (Blepharospasm), or larynx (Spasmodic Dysphonia).

In patients with OMD, involuntary contractions may involve the muscles used for chewing (masticatory muscles). These may include the thick muscle in the cheek that closes the jaw (masseter muscle) and the broad muscle that draws back the lower jaw and closes the mouth (temporalis muscle). Some patients may also experience involuntary contractions of the wide muscle at the side of the neck (platysmal muscle). This muscle draws down the corner of the mouth and lower lip or other muscle groups.


Meige's is commonly misdiagnosed and most doctors will have not seen this condition before. Usually a neurologist who specializes in movement disorders can detect Meige's. There is no way to detect Meige's by blood test or MRI or CT scans. OMD by itself may be misdiagnosed as TMJ.

The lack of prompt response to anticholinergic drugs in cases of idiopathic Meige's syndrome is important in differentiating it from acute dystonia, which does respond to anticholinergics.[2]


The main symptoms involve involuntary blinking and chin thrusting. Some patients may experience excessive tongue protrusion, squinting, light sensitivity, muddled speech, or uncontrollable contraction of the platysma muscle. Some Meige's patients also have "laryngeal dystonia" (spasms of the larynx). Blepharospasm may lead to embarrassment in social situations, and oromandibular dystonia can affect speech, making it difficult to carry on the simplest conversations. This can cause difficulty in both personal and professional contexts, and in some cases may cause patients to withdraw from social situations.

The condition tends to affect women more frequently than men.


In some cases Meige's syndrome can be reversed when it is caused by medication. It has been theorized that it is related to cranio-mandibular orthopedic misalignment, a condition that has been shown to cause a number of other movement disorders (Parkinon's,[4] tourettes,[5] and torticollis[6]). This theory is supported by the fact that the trigeminal nerve is sensory for blink reflex, and becomes hypertonic with craniomandibular dysfunction. Palliative treatments are available, such as botulinum toxin injections.[7]

See also


  1. synd/547 at Who Named It?
  2. 1 2 3 Ananth J, Edelmuth E, Dargan B (April 1988). "Meige's Syndrome Associated with Neuroleptic Treatment". American Journal of Psychiatry. 145 (4): 513–515. PMID 2894781.
  3. Boodman, Sandra G. (April 23, 2012). "Medical mysteries: I opened my laptop and my eyes snapped shut". Washington Post. Retrieved April 24, 2012.
  4. TMDiary (Journal of the American Academy of Craniofacial Pain), Vol 21 No.1 2008, pp.28-33
  5. Tourettes syndrome: a pilot study for the discontinuance of a movement disorder; Sims and Stack; J craniomandibular practice, p 11-18; Jan 2009 vol 27 #1
  6. Spasmotic Torticollis: the dental connection; Sims, Stack, and Dermerjian; Cranio, July 2012, Vol 30 Issue 3
  7. Czyz CN, Burns JA, Petrie TP, Watkins JR, Cahill KV, Foster JA. "Long-term Botulinum Toxin Treatment of Benign Essential Blepharospasm, Hemifacial Spasm, and Meige Syndrome". Am J Ophthalmol. 156 (1): 173–177.e2. doi:10.1016/j.ajo.2013.02.001. PMID 23541393.
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