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  MOVEMENT DISORDERS  
       
 

Parkinson's Disease  
    Parkinson's disease (also known as Parkinson disease or PD) is a degenerative disorder of the central nervous system  
    that often impairs the sufferer's motor skills, speech, and other functions. The disease is named after English apothecary  
    James Parkinson, who made a detailed description of the disease in his essay: "An Essay on the Shaking Palsy" (1817).  
       
  Dystonia  
    Dystonia is a neurological movement disorder in which sustained muscle contractions cause twisting and repetitive  
    movements or abnormal postures. The disorder may be hereditary or caused by other factors such as birth-related  
    or other physical trauma, infection, poisoning (e.g., lead poisoning) or reaction to pharmaceutical drugs, particularly  
    neuroleptics.  
   
 
  Essential Tremor  
    Tremor is involuntary trembling involving a certain part of the body. Essential tremor (ET) is tremor that occurs with  
    purposeful movement (e.g., holding a glass to drink, shaving, writing, or buttoning a shirt). It occurs most often in the  
    hands and head but it also can affect the arms, voice box (larynx), trunk, and legs.  
    Essential tremor is caused by abnormalities in areas of the brain that control movement and does not occur as the result  
    of disease (e.g., Parkinson's disease). ET usually does not result in serious complications.  
       
  Restless Legs Syndrome  
    Restless legs syndrome (RLS), also known as Wittmaack-Ekbom's syndrome or Jimmy Legs is a condition that is  
    characterized by an irresistible urge to move one's body to stop uncomfortable or odd sensations. It most commonly  
    affects the legs, but can also affect the arms or torso, and even phantom limbs. Moving the affected body part  
    modulates the sensations, providing temporary relief.  
       
  Huntington's Disease  
    Huntington's disease is a progressive, degenerative disease that causes certain nerve cells in your brain to waste away.  
    As a result, you may experience uncontrolled movements, emotional disturbances and mental deterioration.  
    Huntington's disease is an inherited disease. Signs and symptoms usually develop in middle age. Younger people with  
    Huntington's disease often have a more severe case, and their symptoms may progress more quickly. Rarely, children may  
    develop Huntington's disease.  
    Medications are available to help manage the signs and symptoms of Huntington's disease, but treatments can't prevent the  
    physical and mental decline associated with the condition.  
       
  Wilson's Disease  
    Wilson's disease is a condition where too much copper builds up in the body. It is a rare inherited disorder that affects  
    about 1 in 30,000 people. It is named after Dr Samual Wilson who first described the disorder in 1912.  
    If you inherit the genetic fault in Wilson's disease, your body is not able to get rid of copper. Copper is a 'trace metal'  
    which is in many foods. You need tiny amounts of copper to remain healthy. Normally, the body gets rid of any excess  
    copper. People with Wilson's disease cannot get rid of excess copper and so it builds up in the body, mainly in the liver,  
    the brain, the cornea and kidneys.  
       
  Inherited Ataxias  
    Ataxia, a medical term originated from the Greek language meaning "without order," refers to disturbances in the control of  
    body posture, motor coordination, speech control, and eye movements. Several brain areas, including the cerebellum and  
    the spinocerebellar tracts, substantia nigra, pons, and cerebral cortex control these functions. Injuries in one or more of  
    these areas or in the spinal cord may lead to some form of ataxia. Birth trauma, medication toxicity, drug abuse, infections,  
    tumors, degenerative disorders, head injury, stroke, or aneurysm, as well as hereditary neurological disorders also may  
    cause ataxia. Many different types of inherited ataxias are presently known. Examples include Machado-Joseph disease,  
    ataxia-telangiectasia, and Friedreich ataxia.  
       
  Tourette Syndrome  
   
Tourette syndrome (TS) is an inherited neurological disorder that typically appears in childhood. The main features of TS
are repeated movements and vocalizations called tics. TS can also be associated with behavioral and developmental
problems.
 
       
  Cerebral Palsy  
    Cerebral palsy (CP) is an umbrella term for a group of disorders affecting body movement, balance, and posture. Loosely  
    translated, cerebral palsy means “brain paralysis.” Cerebral palsy is caused by abnormal development or damage in one or  
    more parts of the brain that control muscle tone and motor activity (movement). The resulting impairments first appear  
    early in life, usually in infancy or early childhood. Infants with cerebral palsy are usually slow to reach developmental  
    milestones such as rolling over, sitting, crawling, and walking.  
    Common to all individuals with cerebral palsy is difficulty controlling and coordinating muscles. This makes even very simple  
    movements difficult.  
    Cerebral palsy may involve muscle stiffness (spasticity), poor muscle tone, uncontrolled movements, and problems with  
    posture, balance, coordination, walking, speech, swallowing, and many other functions.  
    Mental retardation, seizures, breathing problems, learning disabilities, bladder and bowel control problems, skeletal  
    deformities, eating difficulties, dental problems, digestive problems, and hearing and vision problems are often linked to CP  
    The severity of these problems varies widely, from very mild and subtle to very profound.  
 

 

 

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