Complex Movement Disorders

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Article Summary

Complex movement disorders describe any combination of atypical movements that interfere with a person’s desired movements. Kids who have complex movement disorders might experience too much or too little movement, or they might have coordination problems. The term "movement disorders" refers to a group of nervous system (neurological) conditions that cause abnormal increased movements, which may be voluntary or involuntary. Movement disorders can also cause...

Key Takeaways

  • This article explains Types of Complex Movement Disorders in simple medical language.
  • This article explains What Causes Complex Movement Disorders? in simple medical language.
  • This article explains Complex Movement Disorders Symptoms and Effects in simple medical language.
  • This article explains Complex Movement Disorders Diagnosis and Treatment in simple medical language.
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Definition

Complex movement disorders describe any combination of movements that interfere with a person’s desired movements. Kids who have complex movement disorders might experience too much or too little movement, or they might have coordination problems. The term “movement disorders” refers to a group of nervous system (neurological) conditions that cause abnormal increased movements, which may be voluntary or involuntary. Movement disorders can also cause reduced or slow movements.

Types of Complex Movement Disorders

There are several types of complex movement disorders, but most are categorized as:

  • Hypokinetic (too little) movement disorders are rare in children.
  • Hyperkinetic (too much) movement disorders, occur more frequently in children than in adults and include unusual or unwanted movements. The most common types of hyperkinetic disorders in children involve involuntary, repetitive movements and vocalizations (tics) or repetitive movements (stereotypies).

Common hyperkinetic disorders include:

  • Dystonia – Kids who have dystonia have muscles that tighten involuntarily, causing uncontrollable, repetitive, stiff, twisting, or exaggerated motions. Symptoms can range from to and might interfere with daily activities, depending on which areas of the body are affected. Dystonia causes include Brain injury from low oxygen levels in the bloodstream at birth causes . Genetics—some forms of dystonia are . Other disorders or conditions—such as severe after birth, infections, or reactions to certain medicines.
  • Tardive Syndromes – The most common symptoms of this type of movement disorder are slow, repetitive, involuntary movements of the mouth and tongue. Tardive syndromes can also range from twisting movements of the entire body to quick dance-like (also known as choreatic) movements. Often, kids who have this condition also experience a sense of restlessness. Tardive syndromes are caused by exposure to certain antipsychotic medicines (such as haloperidol). Because Tardive syndromes are caused by medication, the symptoms usually appear after a child has been taking the medication for some time.
  • Chorea – The term “chorea” comes from the Greek word meaning “to dance.” This disorder causes brief, irregular, and involuntary movements that appear to flow from one muscle to the next in different parts of the body. The form of chorea seen most often in children is called Sydenham’s chorea. It is extremely rare and occurs after strep (streptococcal) infections. Other rare causes of chorea disease in children include side effects from medication or toxins, , and metabolic conditions.
  • This movement disorder affects the part of the brain that controls coordinated movement (). Ataxia may cause uncoordinated or clumsy balance, speech or limb movements, and other symptoms.
  • dystonia. This condition causes long-lasting contractions (spasms) or intermittent contractions of the neck muscles, causing the neck to turn in different ways.
  • Chorea. Chorea is characterized by repetitive, brief, irregular, somewhat rapid, involuntary movements that typically involve the face, mouth, trunk, and limbs.
  • Dystonia. This condition involves sustained involuntary muscle contractions with twisting, repetitive movements. Dystonia may affect the entire body ( dystonia) or one part of the body (focal dystonia).
  • Functional movement disorder. This condition may resemble any of the movement disorders, but is not due to neurological disease.
  • Huntington’s disease. This is an inherited progressive, neurodegenerative disorder that causes uncontrolled movements (chorea), impaired cognitive abilities and psychiatric conditions.
  • Multiple system . This uncommon, progressive neurological disorder affects many brain systems. Multiple system atrophy causes a movement disorder, such as ataxia or parkinsonism. It can also cause low blood pressure and impaired function.
  • Myoclonus. This condition causes lightning-quick jerks of a muscle or a group of muscles.
  • Parkinson’s disease. This slowly progressive, neurodegenerative disorder causes tremors, (), slow decreased movement (bradykinesia), or imbalance. It may also cause other nonmovement symptoms.
  • Parkinsonism. Parkinsonism describes a group of conditions that has symptoms similar to those of Parkinson’s disease.
  • Progressive supranuclear palsy. This is a rare neurological disorder that causes problems with walking, balance, and eye movements. It may resemble Parkinson’s disease but is a distinct condition.
  • Restless legs . This movement disorder causes unpleasant, abnormal feelings in the legs while relaxing or lying down, often relieved by movement.
  • Tardive dyskinesia. This neurological condition is caused by the long-term use of certain drugs used to treat psychiatric conditions (neuroleptic drugs). Tardive dyskinesia causes repetitive and involuntary movements such as grimacing, eye blinking, and other movements.
  • Tourette syndrome. This is a neurological condition that starts between childhood and teenage years and is associated with repetitive movements (motor tics) and vocal sounds (vocal tics).
  • . This movement disorder causes involuntary rhythmic shaking of parts of the body, such as the hands, head, or other parts of the body. The most common type is essential tremor.
  • Wilson’s disease. This is a rare inherited disorder that causes excessive amounts of copper to build up in the body, causing neurological problems.

What Causes Complex Movement Disorders?

Many factors might increase a child’s risk of developing a complex movement disorder. Some of the most common include:

  • .
  • Birth complications.
  • Brain injury.
  • Side effects from medication.
  • , , tumors, or stroke.
  • Other medical conditions and disorders.
  • Genetics
  • Infections
  • Medicines
  • Damage to the brain, , or peripheral nerves
  • Metabolic disorders
  • Stroke and vascular diseases
  • Toxins

Complex Movement Disorders Symptoms and Effects

Because the symptoms and effects of complex movement disorders in children vary depending on the type of disorder, the impact on quality of life differs from person to person.

Some common symptoms and effects of complex movement disorders include:

  • Difficulty walking or running.
  • Depression, anxiety, and social isolation.
  • Sleep disorders.
  • Speech and language difficulties.
  • Difficulty swallowing, chewing, or eating.
  • Difficulty writing, dressing, and manipulating small objects

Complex Movement Disorders and Treatment

Complex movement disorders can be difficult to diagnose and treat. That’s why Gillette Children’s Specialty Healthcare established a Complex Movement Disorders Clinic which includes specialists from neurology,  medicine, neurosurgery, orthopedics, and rehabilitation therapies.

In most cases, specialists can make a diagnosis by visually examining a child’s movements. Because some complex movement disorders are caused by an underlying health condition or injury, however, additional testing and evaluation might be done to ensure that other medical conditions don’t need to be addressed.

If your child is being evaluated for complex movement disorders, your child might have common diagnosis tests like:

  • Blood and urine analysis.
  • Genetic or DNA tests.
  • Gait and motion analysis.
  • Rehabilitation therapies evaluation.
  • Neurodiagnostic testing, including sleep studies (polysomnography) and electroencephalograms (EEGs).
  • Neuropsychological evaluations—to address concerns with attention, memory, learning, and problem-solving.
  • Nutrition and feeding evaluations, which might include swallowing studies.
  • Radiology and imaging tests.
  • A developmental conducted by a neurologist, pediatric rehabilitation medicine specialist, and neurosurgeon
Because movement disorders can have several causes, our Complex Movement Disorder Clinic includes an interdisciplinary team of specialists who work together to provide expert diagnoses and customized treatment plans. Our goal is to help patients achieve their highest possible levels of independence, comfort, and happiness in a family-centered environment.

Some of the most common treatments and therapies associated with complex movement disorders are:

  • Oral medication.
  • Injected medicines like botulinum toxin and phenol.
  • Implanted baclofen pump.
  • .
  • Occupational therapy.
  • Speech and language therapy.
  • Selective dorsal rhizotomy (SDR) surgery.
  • Deep brain stimulation.

Integrated Care

If your child has a complex movement disorder, your family might see a wide range of specialists who work together to provide a comprehensive treatment plan using state-of-the-art technology.

Your care team at Gillette can help you determine if and when to work with experts in:

  • Neurology.
  • Pediatric orthopedics.
  • Rehabilitation therapies.
  • Sleep medicine.
  • Child life.
  • Neuropsychology.
  • Nutrition and feeding.
  • Psychology.
  • Neuropsychology.
  • Social work.
  • recreation.

Our team of complex movement disorder specialists strives to help your child improve function and enhance their quality of life.

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Prepare before seeing a doctor

A simple rural-patient checklist to help you explain symptoms clearly, ask better questions, and avoid unsafe self-treatment.

Safety note: This is not a prescription or diagnosis. For severe symptoms, pregnancy danger signs, children with serious illness, chest pain, breathing difficulty, stroke-like weakness, or major injury, seek urgent care.

Which doctor may help?

Start with a registered doctor or the nearest qualified health center.

What to tell the doctor

  • Write when the problem started and how it changed.
  • Bring old prescriptions, investigation reports, and current medicines.
  • Write allergies, pregnancy status, diabetes, kidney/liver disease, and major past illnesses.
  • Bring one family member if the patient is weak, elderly, confused, or a child.

Questions to ask

  • What is the most likely cause of my symptoms?
  • Which danger signs mean I should go to hospital quickly?
  • Which tests are necessary now, and which can wait?
  • How should I take medicines safely and what side effects should I watch for?
  • When should I come for follow-up?

Tests to discuss

  • Vital signs: temperature, pulse, blood pressure, oxygen saturation
  • Basic physical examination by a clinician
  • CBC, urine test, blood sugar, or imaging only when clinically needed

Avoid these mistakes

  • Do not use antibiotics, steroid tablets/injections, or strong painkillers without proper medical advice.
  • Do not hide pregnancy, kidney disease, ulcer, allergy, or blood thinner use.
  • Do not delay emergency care when danger signs are present.

Medicine safety and first-aid guide

This section is for patient education only. It does not replace a doctor, pharmacist, or emergency care.

Safe first steps

  • Avoid heavy lifting, sudden bending, and prolonged bed rest.
  • Use comfortable posture and gentle movement as tolerated.
  • Discuss physiotherapy, X-ray, or MRI only when clinically needed.

OTC medicine safety

  • For mild back pain, pain-relief medicine may be discussed with a doctor or pharmacist.
  • Avoid repeated painkiller use if you have kidney disease, stomach ulcer, uncontrolled blood pressure, or are taking blood thinners.

Avoid these mistakes

  • Do not start antibiotics without a proper medical decision.
  • Do not use steroid tablets or injections casually for quick relief.
  • Do not delay emergency care because of home remedies.

Get urgent help if

  • Back pain with leg weakness, numbness around private area, loss of urine/stool control, fever, cancer history, or major injury needs urgent care.
Medicine names, dose, and timing must be decided by a qualified clinician or pharmacist after checking age, pregnancy, allergy, other diseases, and current medicines.

For rural patients and family caregivers

Patient health record and symptom diary

Write your symptoms, medicines already taken, test results, and questions before visiting a doctor. This note stays on your device unless you print or copy it.

Doctor to discuss: Doctor / qualified healthcare provider
Tests to discuss with doctor
  • Basic vital signs: temperature, pulse, blood pressure, oxygen level if needed
  • Relevant blood, urine, imaging, or specialist tests only after clinical assessment
Questions to ask
  • What is the most likely cause of my symptoms?
  • Which warning signs mean I should go to emergency care?
  • Which tests are really needed now?
  • Which medicines are safe for my age, pregnancy status, allergy, kidney/liver/stomach condition, and current medicines?

Emergency warning signs such as chest pain, severe breathing difficulty, sudden weakness, confusion, severe dehydration, major injury, or loss of bladder/bowel control need urgent medical care. Do not wait for online information.

Safe pathway to proper treatment

Care roadmap for: Complex Movement Disorders

Use this simple roadmap to understand the next safe steps. It is educational and does not replace examination by a doctor.

Go to emergency care if you notice:
  • Severe or rapidly worsening symptoms
  • Breathing difficulty, chest pain, fainting, confusion, severe weakness, major injury, or severe dehydration
Doctor / service to discuss: Qualified healthcare provider; specialist depends on symptoms and examination.
  1. Step 1

    Check danger signs first

    If danger signs are present, seek emergency care and do not wait for online information.

  2. Step 2

    Record the symptom story

    Write when symptoms started, severity, medicines already taken, allergies, pregnancy status, and test results.

  3. Step 3

    Visit a qualified clinician

    A doctor, nurse, or qualified healthcare provider can examine you and decide which tests or treatment are needed.

  4. Step 4

    Do only useful tests

    Do tests after clinical assessment. Avoid unnecessary tests, random antibiotics, or repeated medicines without diagnosis.

  5. Step 5

    Follow up and return early if worse

    If symptoms worsen, new warning signs appear, or treatment is not helping, return for review quickly.

Rural patient practical tips
  • Take a written symptom diary and all previous prescriptions/test reports.
  • Do not hide medicines already taken, even herbal or over-the-counter medicines.
  • Ask which warning signs mean urgent referral to hospital.

This roadmap is for education. A real diagnosis and treatment plan requires history, examination, and clinical judgment.