Table of Contents
Introduction
Congenital and genetic syndromes can affect a child’s growth, musculoskeletal development, and overall physical function. Early identification and specialized care are essential to support healthy development, prevent complications, and improve quality of life. Premier Podiatry and Orthopedics offers compassionate, evidence-based care tailored to each child’s unique needs.
Congenital and Genetic Syndromes Affecting the Musculoskeletal System
Several congenital and genetic syndromes can have orthopedic manifestations in children and adolescents, including:
- Down Syndrome: Hypotonia, joint laxity, and an increased risk of cervical spine instability can affect mobility and posture.
- Marfan Syndrome: Characterized by long limbs, joint hypermobility, and scoliosis, which may require monitoring and orthopedic intervention.
- Ehlers-Danlos Syndrome: Connective tissue abnormalities can cause joint hypermobility, frequent sprains, and delayed bone healing.
- Achondroplasia: A form of dwarfism with characteristic limb shortening, spinal stenosis, and joint deformities that require orthopedic attention.
- Osteogenesis Imperfecta: Fragile bones and frequent fractures necessitate specialized orthopedic management and monitoring.
Early recognition of these syndromes allows for proactive care, including physical therapy, orthotic support, and surgical interventions when necessary.
Personalized Pediatric Orthopedic Care
At Premier Podiatry and Orthopedics, Dr. Sheu offers individualized evaluation and treatment plans for children with congenital and genetic syndromes. Care focuses on improving mobility, function, and quality of life.
Recovery and Rehabilitation
Recovery plans are tailored to each child, incorporating physical therapy, bracing, and activity modifications as needed. Dr. Sheu works closely with families to ensure a safe and effective rehabilitation process, promoting long-term musculoskeletal health.
Genetic Resources
Families benefit from access to genetic counseling, educational resources, and support networks to better understand their child’s condition. Collaborating with genetic specialists helps guide treatment decisions and informs monitoring for potential orthopedic complications.
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