What Is Osteogenesis Imperfecta Type 2?

What is an OI baby?

Osteogenesis imperfecta (OI) is a rare inherited (genetic)bone disorder that is present at birth.

It’s also known as brittle bone disease.

A child born with OI may have soft bones that break (fracture) easily, bones that are not formed normally, and other problems.

Symptoms may range from mild to severe..

What body systems are affected by osteogenesis imperfecta?

Osteogenesis imperfecta, also known as brittle bone disease, is a genetic disorder that causes bones to break easily without cause. The condition affects the body’s ability to produce collagen, a protein in the body’s connective tissue.

Can brittle bone disease be cured?

Brittle bone disease is a lifelong genetic disorder that causes your bones to break very easily, usually without any type of injury, as from a fall. Your doctor may also call it osteogenesis imperfecta. It affects both sexes and all races equally. There is no cure for brittle bone disease, but your doctor can treat it.

Can osteogenesis imperfecta be cured?

Because osteogenesis imperfecta (OI) is a genetic condition, it has no cure. For many years, surgical correction of deformities, physiotherapy, and the use of orthotic support and devices to assist mobility (eg, wheelchairs) were the primary means of treatment.

What is OI type 2?

OI type II is the most severe type of osteogenesis imperfecta. Affected infants often experience life-threatening complications at, or shortly after, birth. Infants with OI type II have low birth weight, abnormally short arms and legs (limbs), and bluish discoloration of the whites of the eyes (blue sclera).

What are the four types of osteogenesis imperfecta?

Here are the four main types of OI:Type 1 OI. Type 1 OI is the mildest and most common form of brittle bone disease. … Type 2 OI. Type 2 OI is the most severe form of brittle bone disease, and it can be life-threatening. … Type 3 OI. Type 3 OI is also a severe form of brittle bone disease. … Type 4 OI.

What’s wrong with the Baxter baby?

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.

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.

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 old is the Baxter baby?

Toddler Born With a Rare Condition Is Capturing the Hearts of the Whole Internet. Byron Baxter is a 3-year-old who was born with a rare condition called osteogenesis imperfecta, or brittle bone disease. He’s quickly become a viral star, capturing the attention of celebs like Cardi B.

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.

Who is most likely to get osteogenesis imperfecta?

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.