Chromosome 22 Duplication Syndrome – Panasséa – Pediatric Therapy Centre in Malta

Understanding Chromosome 22 Duplication Syndrome: Personalized Therapy for Lifelong Support

Your child’s journey with Chromosome 22 Duplication Syndrome is unique. At Panasséa, we provide expert, compassionate therapy to help your child reach their full potential—no matter where they are in their development. We walk alongside your family with tailored care, every step of the way.

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What is Chromosome 22 Duplication Syndrome?

Chromosome 22 Duplication Syndrome is a rare genetic condition caused by an extra segment of genetic material on chromosome 22. The duplication can vary in size and position, which means the symptoms and severity can differ greatly from one child to another.

Common challenges associated with this condition include:

Developmental delays
Intellectual disabilities
Low muscle tone (hypotonia)
Speech and language difficulties
Feeding issues
Autism-like behaviors or social communication difficulties
Congenital heart defects or other physical anomalies in some cases

The condition may be diagnosed through genetic testing, often after concerns about developmental milestones arise. With the right support and therapy, children with Chromosome 22 Duplication Syndrome can make meaningful progress in motor, cognitive, and social areas.

Quick Facts:

Caused by a duplication on chromosome 22
Symptoms vary widely, even within families
Early intervention leads to the best developmental outcomes

Why Choose Panasséa?

Specialized Therapy That Adapts to Your Child

At Panasséa, we understand how genetic conditions like Chromosome 22 Duplication Syndrome can affect many aspects of a child’s life. Our team provides a compassionate, coordinated therapy experience designed to meet your child’s evolving needs.

Comprehensive Care: We address motor skills, speech, sensory challenges, and cognitive development.
Individualized Plans: Every child receives a customized therapy approach based on their unique abilities.
Family Involvement: We help parents and caregivers become confident partners in their child’s growth.
Flexible Delivery: Choose from in-clinic sessions, home programs, or telehealth options.
Growth-Focused: We regularly assess and adjust therapy goals to reflect your child’s progress and changing needs.

Services We Offer

Therapy Designed Around Your Child’s Needs

Physical Therapy (PT):
- Supports motor development, posture, balance, and mobility. Especially helpful for children with hypotonia or motor delays.
Occupational Therapy (OT):
- Focuses on fine motor skills, daily living activities (feeding, dressing), and sensory regulation. Helps improve independence.
Speech and Language Therapy:
- Addresses expressive and receptive language delays, articulation, and social communication. May also assist with feeding issues or oral motor delays.
Assistive Technology & Equipment:
- Recommends tools such as adaptive seating, communication devices, or sensory tools to support learning and interaction.
Parent & Caregiver Support:
- Offers guidance, education, and emotional support to help families navigate therapies, routines, and daily challenges.

Explore Our Services in Detail

Understanding the Journey

How We Work With You

Initial Consultation:
- We meet to understand your child’s history, current strengths, and therapy goals. We take the time to listen and connect.
Comprehensive Evaluation:
- In-depth assessments of motor skills, communication, sensory processing, and cognitive development. We tailor everything to your child.
Personalized Therapy Plan:
- We create a goal-based, individualized care plan that includes recommended therapies and home strategies.
Ongoing Care & Review:
- We regularly check in on your child’s progress and adjust goals as needed. You’ll always feel informed and supported.

Common Questions:

Will my child ever talk or walk?
While each child’s progress varies, many children with Chromosome 22 Duplication Syndrome achieve key developmental milestones with early and consistent support.
How is this condition diagnosed?
Through genetic testing, often recommended when delays or multiple health concerns are present.
Can therapy help if my child is already older?
Yes. While early intervention is ideal, therapy at any age can bring meaningful improvement in skills and quality of life.
Do you collaborate with other professionals?
Absolutely. We work closely with pediatricians, geneticists, and educators to ensure coordinated care.

FAQ

Q: Is Chromosome 22 Duplication Syndrome inherited?
A: It can be, but not always. Some duplications occur spontaneously. Genetic counseling can help determine inheritance patterns in your family.

Q: Does my child need long-term therapy?
A: Many children benefit from ongoing therapy, but the level and frequency may change over time based on your child’s development.

Q: Will this affect my child’s schooling?
A: It might. We work with families and schools to ensure children receive the accommodations and support they need to succeed in educational settings.

Q: Can this condition be cured?
A: There is no cure, but with supportive therapies and a loving environment, children can achieve greater independence and participate fully in life.