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What is osteogenesis imperfecta (brittle bone disease)?

Osteogenesis imperfecta (brittle bone disease) is a lifelong genetic condition affecting the body’s ability to make collagen protein, causing fragile and brittle bones. Without the right amount of collagen, bones are weak and highly susceptible to trauma, causing frequent fractures and breaks.

Symptoms include broken bones, bleeding, bruising, frequent nosebleeds, bowed legs, difficulties breathing, scoliosis, fatigue, sensitive skin, short stature, and weak muscles and tissues. While there is no cure, the condition can be managed.

What issues do children with osteogenesis imperfecta face?

PAIN

Weakened bones can lead to abnormal bending, painful breaks, and fractures.

DISCRIMINATION

Children with frequent broken bones are vulnerable to bullying and exclusion.

LIMITED MOBILITY

Children can lose the ability to walk, preventing them from attending school.

How does surgery change a child’s life?

  • The condition can be managed with medicine to strengthen, and surgery to straighten, the bones.
  • Children experience restored confidence and hope as they are accepted into community life.
  • Mobility improves so children can run, play, walk pain-free, and complete school, which leads to more opportunities.

 

Miracles happen every day at CURE Children’s Hospital of Malawi

HOW NOEL OVERCAME BRITTLE BONE DISEASE

Noel’s condition caused his legs to bend and frequently break. After unsuccessful treatments at a local hospital, CURE Malawi provided the surgery he needed at no cost. Because CURE provides comprehensive care, Noel was treated again when his condition returned.

 

Contact Us

CURE Malawi’s mission is to provide every child living with a treatable disability the physical, emotional, and spiritual care they need to heal. If you have questions about becoming a patient or a partner with CURE, please contact us.

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