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Jumping Frenchmen of Maine

NORD is very grateful to Ronald C. Simons, MD, Professor Emeritus, Departments of Psychiatry and Anthropology, Michigan State University; Adjunct Professor, Department of Psychiatry (ret.), University of Washington, for assistance in the preparation of this report.

Synonyms of Jumping Frenchmen of Maine

  • No synonyms found.

Disorder Subdivisions

  • No subdivisions found.

General Discussion

Jumping Frenchmen of Maine is an extremely rare disorder characterized by an unusually extreme startle reaction. The startle reaction is a natural occurrence. It is the normal, rapid, involuntary response to a sudden or unexpected stimulus (e.g., a sudden noise or sight). The exact cause of jumping Frenchmen of Maine is unknown. One theory is that the disorder occurs because of an extreme conditioned response to a particular situation influenced by cultural factors. Jumping Frenchmen of Maine was first identified during the late nineteenth century in Maine and the Canadian province of Quebec among an isolated population of lumberjacks of French Canadian descent. Jumping Frenchmen of Maine is one of a group of culturally specific similar disorders, the startle-matching syndromes, which have been described from various parts of the world. The relationship among these disorders is unknown.


The symptoms of jumping Frenchmen of Maine usually begin after puberty or during the teenage years. Individuals affected by this disorder display an abnormal and exaggerated startle reaction consisting of jumping, screaming, flailing the arms, hitting, or throwing objects.

A startle reaction is caused by sudden or unexpected stimuli such as loud or unexpected noises, a sudden command or gesture, or unexpected physical contact such as a sudden poke in the ribs. Following the startle reaction, affected individuals may repeat back words or phrases in a parrot-like manner (echolalia) and they may involuntarily mimic or imitate movements or gestures (echopraxia). Some affected individuals may involuntarily swear or utter obscene or socially inappropriate words or phrases (coprolalia). In addition, some affected individuals may exhibit automatic or "forced" obedience after a startle response during which they automatically respond to simple commands such as jump, run or hit. Normally, these individuals would not respond to such commands.

In most cases, the symptoms lessened in frequency and severity as affected individuals grew older. The intensity of the startle response may be affected by the frequency of being startled as well as fatigue, stress or emotional tension. An affected individual must be startled in order to elicit the reaction. Jumping Frenchmen of Maine can dramatically impact daily life because of the inability to control or mediate stimuli in the course of one's day. Individuals with jumping Frenchmen of Maine were often teased deliberately causing an increase in the frequency and severity of the episodes. Usually, the more frequently an individual is startled, the more severe and stereotyped is the response.


Although the exact cause of jumping Frenchmen of Maine is unknown, it is believed to be a neuropsychiatric disorder. The startle reaction is a normal human response to sudden or unexpected noise or movement. However, in individuals with jumping Frenchmen of Maine the reaction is exaggerated or abnormal.

Because so few cases of jumping Frenchmen of Maine have been reported and no detailed studies have been conducted, the exact cause(s) and underlying mechanisms of this and similar disorders are unknown. It is possible that both genetic and environmental factors may play a role in the development of these types of disorders.

A few theories have been proposed to explain the development of jumping Frenchmen of Maine. One theory suggests that such disorders are behavioral disorders that develop due to culturally-specific operant conditioning. Operant conditioning is a method of learning a behavior based upon rewards and punishment. An example of operant conditioning is children who learn that they will not able to play until after completing their homework. In such cases, the underlying reasons why individuals develop the exaggerated startle reflect that characterizes the disorder is unknown.

However, some researchers believe that jumping Frenchmen of Maine may be a somatic neurological disorder. A somatic disorder is caused by a gene mutation that occurs after fertilization and is not inherited from the parents or passed on to children. Cultural influences would mediate the severity and expression of such a disorder in individual cases.

More research is necessary to determine the exact causes(s) and underlying mechanisms involved in jumping Frenchmen of Maine and related culturally-specific startle disorders.

Affected Populations

Originally, jumping Frenchmen of Maine was identified in the Moosehead Lake region of Maine among French Canadian lumberjacks. In the reported cases, it affected men more often than women. The disorder seems to have been common in the lumber camps of the region during the nineteenth and early twentieth centuries. However, similar behavior has been observed in specific isolated populations in Louisiana (where it is called Rajun Cajuns), Malaysia (where it is called Latah), Siberia (where it is called Myriachit) as well as India, Somalia, Yemen and the Philippines.

Related Disorders

Symptoms of the following disorders can be similar to those of jumping Frenchmen of Maine. Comparisons may be useful for a differential diagnosis.

Hyperexplexia, also known as Kok disease, is a rare, hereditary, neurological disorder that may affect infants as newborns (neonatal) or prior to birth (in utero). It may also affect children and adults. Individuals with this disorder have an excessive startle reaction to sudden unexpected noise, movement, or touch. Symptoms include extreme muscle tension (stiffness or hypertonia) that can cause the affected person to fall stiffly, like a log, without loss of consciousness. Exaggeration of reflexes (hyperreflexia) and an unstable way of walking (gait) may also occur. The treatment of hyperexplexia is relatively uncomplicated and involves the use of anti-anxiety and anti-spastic medicines. Because the disorder is frequently misdiagnosed as a form of epilepsy, the process of getting an accurate diagnosis may be prolonged. (For more information on this disorder, choose "hyperexplexia" as your search term in the Rare Disease Database.)

Tourette syndrome is a neurologic movement disorder that is characterized by repetitive motor and vocal tics. The first symptoms usually occur during childhood are rapid eye blinking or facial grimaces. Symptoms may also include involuntary movements of the extremities, shoulders, face and voluntary muscles. Some people with Tourette syndrome may vocalize involuntarily; these may be inarticulate sounds or words. Tourette syndrome is not a progressive or degenerative disorder; symptoms tend to be variable and follow a chronic waxing and waning course. Onset usually occurs before the age of 16. (For more information on this disorder, choose "Tourette" as your search term in the Rare Disease Database.)

An abnormal or exaggerated startle response may also occur due to post-traumatic stress disorder, alcohol or drug withdrawal, anxiety disorders, and certain mental disorders such as schizophrenia.

Standard Therapies

A diagnosis of a startle disorder is suspected based upon a thorough clinical evaluation, a detailed patient history, and a variety of specialized tests to rule out other conditions.

There is no specific therapy for individuals with jumping Frenchmen of Maine. Eliminating the practice of intentionally startling and/or teasing an individual so as to cause a jumping response can help to reduce or end episodes. Symptoms tend to get milder with age, but more intense with stress or anxiety. In the reported cases, startle episodes corresponded with stressful situations such as the start of work as a lumberjack. When affected individuals left the lumberjack camp the disorder lessened in both severity and frequency.

Investigational Therapies

Information on current clinical trials is posted on the Internet at All studies receiving U.S. Government funding, and some supported by private industry, are posted on this government web site.

For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:

Tollfree: (800) 411-1222
TTY: (866) 411-1010

For information about clinical trials sponsored by private sources, contact:

For information about clinical trials conducted in Europe, contact:

Jumping Frenchmen of Maine Resources



Thompson PD. The Phenomenology of Startle, Latah, and Related Conditions. In: Hallet S, Fahn S, Jankovic J, et al., eds. Psychogenic Movement Disorders. Neurology and Neuropsychiatry. Philadelphia: Lippincott, Williams & Wilkins; 2006:48-51.

Simons, RC. Boo! - Culture, Experience, and the Startle Reflex, Oxford University Press, New York and Oxford;1996:204-209.

Menkes JH, Pine Jr JW, et al. Eds. Textbook of Child Neurology. 5th ed. Williams & Wilkins. Baltimore, MD; 1995:166-167.

Bakker MJ, van Dijk JG, van den Maagdenberg AMJM, Tijssen MAJ. Startle syndromes. Lancet Neurol. 2006;5:513-524.

Saint-Hilaire MH, Saint-Hilaire JM. Jumping Frenchmen of Maine. Mov Disord. 2001;16:530.

Howard R, Ford R. From the jumping Frenchmen of Maine to post-traumatic stress disorder: the startle response in neuropsychiatry. Psychol Med. 1992;22:695-707.

Saint-Hilaire MH, Saint-Hilaire JM, Granger L. Jumping Frenchmen of Maine. Neurology. 1986;36:1269-1271.

McKusick VA., ed. Online Mendelian Inheritance in Man (OMIM). Baltimore. MD: The Johns Hopkins University; Entry No:244100; Last Update:11/01/1999. Available at: Accessed:March 5, 2013.

The information in NORD’s Rare Disease Database is for educational purposes only. It should never be used for diagnostic or treatment purposes. If you have questions regarding a medical condition, always seek the advice of your physician or other qualified health professional. NORD’s reports provide a brief overview of rare diseases. For more specific information, we encourage you to contact your personal physician or the agencies listed as “Resources” on this report.

Report last updated: 2013/03/12 00:00:00 GMT+0

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