Congrats Shaan On Publishing
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How to Recognize Pediatric Movement Disorders in Your Child
Medically Reviewed by: Catherine A. Mazzola, MD, FAANS Pediatric Neurosurgeon
Updated On: 18 March 2025
As parents, we strive to safeguard our children’s health and happiness. Sometimes, subtle signs in their movements or behaviors may signal underlying concerns. Pediatric movement disorders are conditions that affect a child's ability to control their movements, ranging from mild clumsiness to pronounced motor difficulties. Early recognition is crucial to ensure timely diagnosis and treatment. This guide from New Jersey Pediatric Neuroscience Institute (NJPNI) explores how to recognize the signs of pediatric movement disorders, common conditions, diagnostic processes, and available expert care.

What Are the Early Signs of Pediatric Movement Disorders?

Pediatric movement disorders can manifest in various ways. Being aware of these early signs can help you act promptly:
  • Muscle Stiffness: Persistent tension or tightness in your child’s muscles or difficulty relaxing their posture may indicate a movement disorder.
  • Tremors: Unintentional shaking, especially during rest or voluntary movements, is a red flag.
  • Involuntary Movements: Sudden, uncontrollable jerking, twisting, or repetitive motions can disrupt daily activities.
  • Balance and Coordination Issues: Frequent stumbling, falling, or trouble with fine motor tasks warrants attention.
  • Speech and Swallowing Difficulties: Some movement disorders can impair clear speech or safe swallowing.

Common Pediatric Movement Disorders

Understanding the specific conditions under the umbrella of pediatric movement disorders can help you seek appropriate care.

1. Spasticity

  • Cause: Often results from brain damage during pregnancy or early childhood. May be associated with prematurity or stroke.
  • Impact: Affects muscle control, posture, and coordination.

2. Dystonia

  • Symptoms: Persistent muscle contractions cause abnormal postures or repetitive movements.
  • Affected Areas: Can involve any body part, making daily activities challenging.

3. Tourette Syndrome

  • Characteristics: Involves motor tics and involuntary vocalizations.
  • Onset: Typically starts in childhood, with varying severity.

4. Ataxia

  • Effect: Impairs coordination and balance.
  • Causes: May stem from genetic factors or neurological conditions, making fine motor skills difficult.

5. Chorea

  • Effect: Impairs coordination.
  • Causes: May stem from genetic factors or neurological conditions, making fine motor skills difficult.

How Are Pediatric Movement Disorders Diagnosed?

If you suspect a movement disorder in your child, seeking professional guidance is crucial. The diagnostic process includes:

1. Medical History Review

  • Discuss family history and developmental milestones with the doctor to gain a comprehensive understanding.

2. Physical Examination

  • The physician assesses muscle tone, reflexes, and coordination to evaluate motor function.

3. Imaging and Tests

  • Advanced tests like MRI scans or blood work may be conducted to confirm the diagnosis or rule out other conditions.

Navigating Pediatric Movement Disorders with NJPNI Specialists

The New Jersey Pediatric Neuroscience Institute (NJPNI) specializes in diagnosing and treating pediatric movement disorders. Here’s why NJPNI stands out:
  • Comprehensive Care Team: Pediatric neurologists,physiatrists, neurosurgeons, physical therapists, and speech therapists collaborate to create tailored treatment plans.
  • Advanced Techniques: Cutting-edge diagnostic tools and therapeutic strategies are employed to address each child’s unique needs.
Early Intervention Focus: Prompt treatment enhances outcomes and ensures optimal development for children.

Conclusion

Recognizing pediatric movement disorders early can make a world of difference in your child’s quality of life. By staying informed about the signs, seeking timely diagnosis, and relying on expert care from institutions like NJPNI, you can support your child’s journey toward better health and well-being. The team at NJPNI is here to guide you every step of the way, offering compassionate care tailored to your child’s needs. Together, we can help your child achieve their full potential.
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How to Reduce Risks and Support Children With Hydrocephalus
Pediatric hydrocephalus is a challenging condition for children and their families. It happens when too much fluid builds up in a child’s brain, creating pressure that can lead to serious health issues. While many children with hydrocephalus go on to lead fulfilling lives, the condition can be life-threatening if not diagnosed or treated in time. This guide explains why morbidity rates in pediatric hydrocephalus are high, what the risk factors are, and how expert care can help. We’ll also highlight the New Jersey Pediatric Neuroscience Institute (NJPNI) and its role in supporting families.

What Is Pediatric Hydrocephalus?

Hydrocephalus is a condition where cerebrospinal fluid (CSF) builds up in the brain, causing swelling and increased pressure. In children, it can happen due to birth defects, infections, or even brain tumors. If hydrocephalus is left untreated, it can lead to severe complications, including developmental delays, seizures, and even death. However, with proper treatment and care, many children live healthy, happy lives.

Why Are Morbidity Rates High in Pediatric Hydrocephalus?

Several factors contribute to the higher risk of morbidity and mortality in children with hydrocephalus: Delayed Diagnosis: Symptoms like an enlarged head or irritability in infants might be missed, delaying critical treatment. Infections: Infections such as meningitis can make hydrocephalus worse, increasing the chances of complications. Shunt Problems: A common treatment for hydrocephalus is a shunt, which helps drain excess fluid from the brain. However, shunts can malfunction or get infected, which can be life-threatening if not addressed quickly. Other Health Issues: Children with hydrocephalus often have other medical problems, which can complicate their care and increase risks.

What Are the Risk Factors for Hydrocephalus in Children?

Understanding what puts a child at risk for hydrocephalus can help parents act early: Congenital Causes: Some babies are born with hydrocephalus due to genetic factors or issues during pregnancy. Infections: Illnesses like meningitis during pregnancy or early infancy can lead to hydrocephalus. Premature Birth: Premature babies are at higher risk due to brain bleeding (intraventricular hemorrhage). Brain Tumors or Injuries: Any blockage in the brain caused by tumors or trauma can lead to fluid buildup.

Can a Child With Hydrocephalus Live a Normal Life?

Yes, with early treatment and ongoing care, many children with hydrocephalus grow up to live fulfilling lives. Treatment Options: A shunt or a procedure like endoscopic third ventriculostomy (ETV) can help manage fluid buildup. Regular checkups ensure the treatment is working and prevent complications. Long-Term Support: Rehabilitation therapies can help with developmental delays. Emotional and educational support ensures children thrive at school and home. The key is catching the condition early and working closely with a pediatric neurosurgeon.

How Can Parents Support a Child With Hydrocephalus?

Supporting a child with hydrocephalus involves more than just medical care—it’s about emotional and practical guidance. The New Jersey Pediatric Neuroscience Institute (NJPNI) provides: Expert Medical Care: Their team of pediatric neurosurgeons specializes in managing hydrocephalus with state-of-the-art treatments. Family Support: They offer resources to help parents understand the condition and make informed decisions. Guidance for Daily Life: NJPNI helps families build care plans that ensure children stay healthy and happy.

Parents can also:

Watch for signs of shunt malfunction, like headaches or nausea. Attend all follow-up appointments. Work with schools to accommodate their child’s needs.

Conclusion: Hope for Children With Hydrocephalus

While pediatric hydrocephalus is a serious condition, timely diagnosis and expert care can make a world of difference. Parents play a vital role in spotting symptoms early and seeking the right treatment. The New Jersey Pediatric Neuroscience Institute offers families the specialized care and support they need to navigate this journey. By working together, we can reduce mortality rates and give children with hydrocephalus the chance to live fulfilling lives. If you suspect your child has hydrocephalus or need guidance, don’t wait—reach out to NJPNI today for compassionate, expert care.

Medically Reviewed By:

Dr. John Collins

MD, DDS, Board-certified Oral and Maxillofacial Surgeon

Reviewed on: October 27, 2023

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NOTICE: This website is for informational purposes only and is not intended as medical advice or as a substitute for a patient/physician relationship.

NJPNI is committed to creating a culturally diverse, inclusive and collaborative community for patients and their families, employees and associates where each person is celebrated and has a sense of equal belonging. See our DEI Statement Page for more information.

NJPNI does not exclude, deny benefits to, or otherwise discriminate against any person on the grounds of race, color, or national origin, or on the basis of disability or age in admission to, participation in, or receipt of the services and benefits of any of its programs and activities or in employment therein. This statement is in accordance with the provisions of Title VI of the Civil Rights Act of 1964, Section 504 of the Rehabilitation Act of 1973, the Age Discrimination Act of 1975, and Regulations of the U.S. Department of Health and Human Services issued pursuant to the Acts, Title 45 Code of Federal Regulations part 80, 84, and 91.

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