- What parts of the body does osteogenesis imperfecta affect?
- Is Osteogenesis Imperfecta painful?
- How can osteogenesis imperfecta be prevented?
- What is an OI baby?
- What is wrong with Byron the Baxter boy?
- What are the causes of osteogenesis imperfecta?
- Can you develop osteogenesis imperfecta?
- Where is osteogenesis imperfecta most common?
- How long can a person with osteogenesis imperfecta live?
- Is Oi a disability?
- How common is Oi?
- How is osteogenesis imperfecta diagnosed?
- What is the hardest bone to heal?
- What is Oi medical condition?
- Is Osteogenesis Imperfecta a type of dwarfism?
- What disease does Byron Baxter have?
- What is osteogenesis imperfecta Type 4?
What parts of the body does osteogenesis imperfecta affect?
In more severe forms of osteogenesis imperfecta, there may be bone deformities, poor lung development and lung problems, a barrel-shaped chest, poor muscle development in the arms and legs.
Osteogenesis imperfecta is caused by a faulty gene that affects the body’s ability to produce collagen..
Is Osteogenesis Imperfecta painful?
Conclusions: Pain is a common occurrence for children with OI and is both acute and chronic in nature, interfering with children’s daily living activities. OI pain may not be optimally treated because many children experienced moderate to severe pain despite use of analgesics and/or coping strategies.
How can osteogenesis imperfecta be prevented?
Light exercise and low impact physical activity like swimming and walking are suggested to keep the muscles strong and agile, and strengthen the bones. In severe OI cases, inserting a metal rod through surgery or bracing is suggested to strengthen the bone and reduce the risk of fractures.
What is an OI baby?
Your child has been diagnosed with osteogenesis imperfecta (OI). This is a rare condition that causes bones to be very thin and delicate so they break (fracture) easily. OI is sometimes called brittle bone disease. There are four types of OI that range from mild to severe.
What is wrong with Byron the Baxter boy?
Boy born with rare condition inspires celebrities, people from around the world. When you listen to 3-year-old Byron Baxter laugh and talk, you’d never know anything was wrong with him. But he was born with a rare condition called osteogenesis imperfecta, or brittle bone disease.
What are the causes of osteogenesis imperfecta?
Osteogenesis imperfecta is a genetic disorder that causes increased bone fractures and collagen defects. The main causes for developing the disorder are a result of mutations in the COL1A1 and COL1A2 genes which are responsible for the production of collagen type 1.
Can you develop osteogenesis imperfecta?
It’s present at birth and usually develops in children who have a family history of the disease. The disease is often referred to as osteogenesis imperfecta (OI), which means “imperfectly formed bone.” Brittle bone disease can range from mild to severe. Most cases are mild, resulting in few bone fractures.
Where is osteogenesis imperfecta most common?
Four main types of OI have been identified. OI type I is the most common and the mildest form of the disorder. OI type II is the most severe. In most cases, the various forms of osteogenesis imperfecta are inherited as autosomal dominant traits.
How long can a person with osteogenesis imperfecta live?
The outlook for people with OI varies greatly for each type of the disease. Most children born with type I OI live normal, healthy lives into adulthood. Less severe symptoms do not affect life expectancy. Most OI-related deaths result from respiratory failure due to weak lungs.
Is Oi a disability?
Most people with OI experience physical disability. OI also can cause weak muscles, brittle teeth, a curved spine, and hearing loss. Most forms of OI are caused by abnormal genes that are passed down from one or both parents to their children. There are currently 11 types of OI.
How common is Oi?
OI occurs in approximately 1 in 20,000 individuals, including people diagnosed after birth. OI occurs with equal frequency among males and females and among racial and ethnic groups. Life expectancy varies depending on how severe the OI is, ranging from very brief (lethal form, OI type II) to average.
How is osteogenesis imperfecta diagnosed?
Tools for diagnosing osteogenesis imperfecta can include:a complete medical history and physical exam (including ear, nose and throat exam to detect hearing loss*)x-rays.DNA blood test.DXA bone density scan.
What is the hardest bone to heal?
Treatments ranging from casting to surgery can be required. Unfortunately, the scaphoid bone has a track record of being the slowest or one of hardest bones to heal.
What is Oi medical condition?
Osteogenesis imperfecta (OI) is a group of genetic disorders that mainly affect the bones. The term “osteogenesis imperfecta” means imperfect bone formation.
Is Osteogenesis Imperfecta a type of dwarfism?
Osteogenesis imperfecta (OI) Type III is a dwarfism condition, with adults generally reaching a height of three feet, although profound short stature is often associated with the other three types as well.
What disease does Byron Baxter have?
That’s because Byron is living with a brittle bone disease, a rare genetic condition with no cure. Doctors call it osteogenesis imperfecta, which means “imperfectly formed bone.”
What is osteogenesis imperfecta Type 4?
Osteogenesis imperfecta type IV is a moderate type of osteogenesis imperfecta (OI; see this term), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures.