DiGeorge Syndrome (22q11.2 Deletion Syndrome)

Understanding DiGeorge Syndrome: Personalized Therapy for Growing Stronger Every Day

Your child’s journey with DiGeorge Syndrome is unique—but you don’t have to navigate it alone. At Panasséa, we provide thoughtful, individualized therapy that meets your child where they are and helps them grow with confidence, communication, and resilience.

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What is DiGeorge Syndrome?

DiGeorge Syndrome, also known as 22q11.2 Deletion Syndrome, is a genetic disorder caused by the deletion of a small piece of chromosome 22. It affects multiple systems in the body and presents a wide range of challenges that vary from child to child. These may include congenital heart defects, immune deficiencies, developmental delays, and learning difficulties.

Some of the most common features include:

  • Delayed speech and language development
  • Feeding and swallowing difficulties
  • Low muscle tone and motor delays
  • Behavioral and attention challenges
  • Immune system problems
  • Cleft palate or other structural abnormalities
  • Learning disabilities or intellectual delays

Children with DiGeorge Syndrome may face a combination of medical, developmental, and educational needs. Therapy plays a key role in supporting them through early milestones, school readiness, and beyond.

Quick Facts:

  • Caused by a deletion on chromosome 22 (22q11.2)
  • Affects approximately 1 in 4,000 children
  • Presents a wide range of symptoms that may vary in severity
  • Early and ongoing therapy significantly improves outcomes

Why Choose Panasséa?

Specialized Therapy That Adapts to Your Child

We know that no two children with DiGeorge Syndrome are alike. Our therapists take the time to understand your child’s unique profile and build a customized therapy plan that addresses developmental, physical, and emotional needs.

  • Whole-Child Approach: We consider all areas of development, from motor skills to communication and sensory integration.
  • Cross-Disciplinary Team: Our therapists collaborate across specialties to deliver integrated care.
  • Experience with Genetic Conditions: We’ve supported many children with rare syndromes and complex medical needs.
  • Family Collaboration: We empower caregivers with tools, resources, and support to encourage growth at home.
  • Flexible Options: Choose in-clinic sessions, home programs, or remote therapy depending on your family’s needs.

Services We Offer

Therapy Designed Around Your Child’s Needs

  1. Physical Therapy (PT):
    • Builds strength, balance, and coordination. Focuses on achieving gross motor milestones like walking, sitting, and postural control.
  2. Occupational Therapy (OT):
    • Supports fine motor skills, self-care tasks, sensory integration, and adaptations for play and learning.
  3. Speech and Language Therapy:
    • Assists with articulation, expressive and receptive language, and supports feeding or swallowing challenges when present.
  4. Feeding & Oral Motor Therapy:
    • Addresses issues such as weak oral muscles, delayed chewing or swallowing, and food aversions.
  5. Parent & Caregiver Support:
    • Personalized coaching, emotional support, and training to continue your child’s progress at home.

Understanding the Journey

How We Work With You

  1. Initial Consultation:
    • We meet with you to understand your child’s medical history, strengths, and priorities. Together, we outline a therapy plan.
  2. Comprehensive Evaluation:
    • Our therapists assess developmental milestones, communication, motor skills, sensory needs, and daily functioning.
  3. Personalized Therapy Plan:
    • A flexible roadmap with clearly defined goals, recommended session frequency, and suggestions for home-based support.
  4. Ongoing Care & Review:
    • We regularly review progress and adjust therapy goals as your child grows. We stay connected with you every step of the way.

Common Questions:

  • Can therapy begin even if my child has medical needs?
    Yes. We tailor our approach based on your child’s health status and collaborate with medical professionals as needed.
  • How long will my child need therapy?
    It varies. Some children benefit from long-term therapy, while others may meet their goals and reduce frequency over time.
  • Can you work with my child’s school team?
    Absolutely. We support IEP planning and coordinate with teachers to align therapy with academic goals.
  • Will my child talk eventually?
    Many children with DiGeorge Syndrome develop speech with time and support. We also offer augmentative communication options when needed.

FAQ

Q: Is DiGeorge Syndrome the same in every child?
A: No. The severity and type of symptoms vary widely. Each child has a unique developmental path.

Q: Is this a progressive condition?
A: No, but your child’s needs may change as they grow. Therapy should evolve alongside them.

Q: What’s the most important area to focus on?
A: That depends on your child’s needs—some may need early feeding therapy, others may focus on motor skills or speech.

Q: Will my child go to a regular school?
A: Many children with DiGeorge Syndrome attend mainstream schools with individualized support and accommodations.


Educational Resources:

DiGeorge Syndrome (22q11.2 Deletion Syndrome)

Downloadable Guides:

  • “Understanding 22q11.2 Deletion Syndrome”
  • “Heart, Immunity, and Feeding Support”

Videos:

  • “Therapy Planning for Multi-System Needs”
  • “Improving Speech and Social Communication”

Blog Posts & Articles:

  • “Supporting Siblings of Children with Complex Needs”
  • “How to Advocate During Medical Appointments”

Book an Appointment

Take the First Step Towards Support

We’re here to help your family thrive. Contact us today to start your journey toward meaningful progress.

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Contact Us

Have questions or want to schedule a consultation?

  • Phone: +356 77 090 183
  • Email: contact@panassea.com
  • Address: 50 Erin Serracino Inglott Street, Iklin IKL 1401, Malta
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