Skip to main content

Jumping Frenchmen of Maine

 Jumping Frenchmen of Maine



OVERVIEW

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.

SYMPTOMS

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.

CAUSES

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.

DISORDERS WITH SIMILAR SYMPTOMS

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.

DIAGNOSIS

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.

STANDARD THERAPIES

Treatment

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.

Type of Doctor Department :Nneurologist

Comments

Popular posts from this blog

Charge Syndrome

Overview CHARGE syndrome is a recognizable genetic syndrome with known pattern of features. It is an extremely complex syndrome, involving extensive medical and physical difficulties that differ from child to child. CHARGE syndrome is correlated with genetic mutation to CHD7 and the prevalence of CHARGE syndrome is 1:10,000-1:15,000 live births. Babies with CHARGE syndrome are often born with life-threatening birth defects. They spend many months in the hospital and undergo many surgeries and other treatments. Swallowing and breathing problems make life difficult even when they come home. Most have hearing two little girls sitting on a carpet, one girl has a trach and is biting her finger.loss, vision loss, and balance problems that delay their development and communication. Despite these seemingly insurmountable obstacles, children with CHARGE syndrome often far surpass their medical, physical, educational, and social expectations. One of the hidden features of CHARGE syndrome is the ...

Legg–Calve–Perthes disease

  Legg–Calve–Perthes disease Overview Legg-Calve-Perthes (LEG-kahl-VAY-PER-tuz) disease is a childhood condition that occurs when blood supply to the ball part (femoral head) of the hip joint is temporarily interrupted and the bone begins to die. This weakened bone gradually breaks apart and can lose its round shape. The body eventually restores blood supply to the ball, and the ball heals. But if the ball is no longer round after it heals, it can cause pain and stiffness. The complete process of bone death, fracture and renewal can take several years. To keep the ball part of the joint as round as possible, doctors use a variety of treatments that keep it snug in the socket portion of the joint. The socket acts as a mold for the fragmented femoral head as it heals. Symptoms Symptoms of Perthes disease include: Limping. Pain or stiffness in the hip, groin, thigh or knee. Limited range of motion of the hip joint. Pain that worsens with activity and improves with rest. Perthes diseas...

Kernicterus

  Kernicterus Overview Kernicterus is a rare condition that affects your baby’s brain when they have too much bilirubin in their blood (hyperbilirubinemia). Bilirubin is a yellow waste product that your body makes. Sometimes, your liver can’t remove enough bilirubin to keep you healthy. Too much bilirubin can cause jaundice. This is when your skin, the whites of your eyes and your gums or the area underneath your tongue (mucous membranes) appear yellow. Symptoms of kernicterus progress in stages. In addition to jaundice, symptoms usually affect newborns and include irritability, poor feeding and seizures. Complications can lead to hearing loss and permanent brain damage. If you notice changes to your newborn’s behavior or appearance, contact their healthcare provider immediately. You may hear your healthcare provider call kernicterus “bilirubin encephalopathy.” Jaundice is common in newborns. Healthcare providers will monitor newborn jaundice to decrease your baby’s risk of develop...