Osteogenesis Imperfecta

Osteogenesis Imperfecta is a genetic condition causing fragile bones and recurrent fractures. At Aarshiva Hospital and ICU, we provide comprehensive management including fracture care, deformity correction, and rodding procedures to reduce fracture risk and improve long-term mobility.

Osteogenesis Imperfecta Treatment in Children

Osteogenesis Imperfecta (OI), commonly known as brittle bone disease, is a genetic disorder characterized by fragile bones that break easily, often with minimal trauma. Children with OI require specialized orthopedic care to manage fractures, prevent deformities, and improve functional mobility.

At Aarshiva Hospital and ICU, we offer comprehensive evaluation and long-term management plans tailored to each child’s condition and severity.


Symptoms of Osteogenesis Imperfecta

  • Frequent bone fractures

  • Bone deformities

  • Short stature

  • Joint laxity

  • Delayed motor development

Early diagnosis and structured care significantly improve quality of life.


Our Treatment Approach

1️⃣ Fracture Management

Prompt and specialized treatment of fractures to ensure proper healing while minimizing complications.

2️⃣ Deformity Correction

Surgical correction of bone deformities to improve alignment and functional ability.

3️⃣ Rodding Procedures

Intramedullary rodding surgery strengthens long bones, reduces fracture frequency, and improves stability.

4️⃣ Long-Term Follow-Up

Regular monitoring of bone growth, mobility, and fracture risk to adjust treatment as needed.


Goals of Treatment

  • Reduce frequency of fractures

  • Improve bone strength and alignment

  • Enhance mobility and independence

  • Prevent progressive deformities

  • Support overall growth and development

At Aarshiva Hospital and ICU, our multidisciplinary approach focuses on improving functional outcomes and helping children with Osteogenesis Imperfecta lead active and fulfilling lives.