How Common Is Osteogenesis Imperfecta Type 2?

What is the life expectancy of someone with osteogenesis imperfecta?

Outlook / Prognosis 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.

The most severe types will result in death at birth or soon after..

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.

Does brittle bone disease affect teeth?

Osteogenesis Imperfecta (OI) is always associated with bone fragility. In addition, OI may affect the growth of the jaws and may or may not affect the teeth. About half of the people who have OI have teeth that appear normal, and their major concerns are routine care.

Is Osteogenesis Imperfecta more common in ethnicity?

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.

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 osteogenesis imperfecta Type 4?

Disease definition. 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.

Does osteogenesis imperfecta qualify for disability?

Although Type II Osteogenesis Imperfecta is one of the 88 conditions that qualifies a disability claim for processing under the Compassionate Allowances guidelines, that does not mean that your child’s claim will be automatically approved by the Social Security Administration.

Is osteogenesis imperfecta Type 2 genetic?

In most cases, osteogenesis imperfecta types I, II, and IV are inherited as autosomal dominant traits. Most cases of OI type II occur without a previous family history of the disorder, resulting instead from a spontaneous genetic change (i.e., new mutation). The inheritance of this mutation is autosomal dominant.

Is Osteogenesis Imperfecta painful?

Background: Pain is a common symptom of osteogenesis imperfecta (OI) among children and adolescents.

Do baby bones break easily?

The good news: Because a baby’s or toddler’s bones are more flexible than an adult’s, they actually don’t break as easily (they tend to bend or buckle instead). Small-fries also heal much more quickly than grown-ups, which means they’ll be up and running (or crawling or cruising) before you know it.

Who is most likely to get osteogenesis imperfecta?

Osteogenesis imperfecta occurs equally in girls and boys and among all racial and ethnic groups, affecting six to seven people in every 100,000. An estimated 20,000 to 50,000 people in the U.S. have the condition. The estimated number varies greatly because milder forms of osteogenesis imperfecta can go undiagnosed.

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.

What is OI Type 3?

Osteogenesis imperfecta type III is a severe type of osteogenesis imperfecta (OI; see this term), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures.

How long do you live with brittle bone disease?

It is estimated that approximately 25,000 to 50,000 people in the U.S. have OI. With good medical management and supportive care, the majority of people who have OI will lead healthy, productive lives and can expect an average lifespan. People with OI experience frequent broken bones from infancy through puberty.

What percent of the population has osteogenesis imperfecta?

Osteogenesis imperfecta affects approximately 1 in 10,000 to 20,000 people worldwide. An estimated 25,000 to 50,000 people in the United States have the condition.

Does osteogenesis imperfecta get worse with age?

It causes bones to break easily. In type 3 OI, your child’s body produces enough collagen but it’s poor quality. Your child’s bones can even begin to break before birth. Bone deformities are common and may get worse as your child gets older.

What is the cause of OI?

What causes osteogenesis imperfecta (OI)? OI is caused by defects in or related to a protein called type 1 collagen (pronounced KOL-uh-juhn). Collagen is an essential building block of the body. The body uses type 1 collagen to make bones strong and to build tendons, ligaments, teeth, and the whites of the eyes.

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.