How Old Is Byron Baxter

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. Likewise, What disease does Byron Baxter have? 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. Also Asked, What happened Byron Baxter? Byron has Osteogenesis Imperfecta which is commonly known as Brittle Bone Disease. Despite his age, he hasn't grown past the size of a toddler and he has broken over 100 bones in his body.

how old is byron baxter

Similar Questions

How many kids are in the Baxter family?

In the process, all five Baxter Children learn how to make new friends and that adventure awaits in the everyday.

How long does someone with osteogenesis imperfecta live?

Life expectancy varies greatly depending on OI type. Babies with Type II often die soon after birth. Children with Type III may live longer, but often only until around age 10. They may also have severe physical deformities.

What is the life expectancy of someone with brittle bone disease?

Life expectancy for males with OI was 9.5 years shorter than that for the general population (72.4 years vs 81.9 years), and for females, was 7.1 years shorter than that for the general population (77.4 years vs 84.5 years).

Did something happen to the Baxter baby?

The quite shocking incident is reported from Georgia where the Lawrenceville family is going through trauma after losing their son Cyrus Baxter, he has passed away on 9th September 2021 due to a road accident and ever since, his family gets too familiar with the news a wave of grief surrounded them.

Who passed away in the Baxter family?

. The Baxter Boys YouTube channel, which has 122,000 subscribers, is run by the family. It has brought attention to Cyrus’s brother, Byron’s, plight.

What causes osteogenesis imperfecta?

Causes and Risk Factors

Osteogenesis imperfecta is caused by a faulty gene that affects the body’s ability to produce collagen. The quantity of collagen produced is either lower or of a poorer quality. If one parent has osteogenesis imperfecta, a child has a 50% chance of having the condition.

Is osteogenesis imperfecta autosomal dominant?

When caused by mutations in the COL1A1 or COL1A2 gene, osteogenesis imperfecta has an autosomal dominant pattern of inheritance, which means one copy of the altered gene in each cell is sufficient to cause the condition.

Can you grow out of brittle bone disease?

There is no cure for brittle bone disease, but treatment can relieve symptoms, prevent breakage of bones, and maximize movement. Severe forms of the disease can affect the shape of the rib cage and spine, which can lead to life-threatening breathing problems.

Why is sclera blue in osteogenesis imperfecta?

Blue sclera is the most commonly known ocular sign for osteogenesis imperfecta and it is caused by thin scleral collagen allowing the underlying darker choroid vasculature to be seen. Patients with OI have shown a reduction in thickness of the corneal and scleral collagen fibers which can result in low ocular rigidity.

What is the average age of death?

According to the most recent data available from the Centers for Disease Control and Prevention, life expectancy at birth in the United States is 77.3 years—74.5 years for men and 80.2 years for women.

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.

Can osteogenesis imperfecta be detected in the womb?

If OI is moderate or severe, healthcare providers usually diagnose it during prenatal ultrasound at 18 to 24 weeks of pregnancy. If a parent or sibling has OI, a healthcare provider can test the DNA of the fetus for the presence of an OI mutation.

Does osteogenesis imperfecta affect the brain?

Cranial complications of osteogenesis imperfecta include a wide range of abnormalities of the skull and brain parenchyma.

What is OI type 3 severe?

Type III. Most severe type in babies who don’t die as newborns. At birth, a baby may have slightly shorter arms and legs than normal and arm, leg, and rib fractures. A baby may also have a larger than normal head, a triangle-shaped face, a deformed chest and spine, and breathing and swallowing problems.

Does everyone have Sutural bones?

They vary in number, shape and size among different population. Approximately 40% of skulls have sutural bones in the lambdoid suture, and occasionally present at the pterion which called pterion ossicle or epipteric bone.

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. Hearing loss is common among adults.

Can OI 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 denomination is Karen Kingsbury?

Karen Kingsbury (born June 8, 1963) is an American Christian novelist born in Fairfax, Virginia. She was a sports writer for the Los Angeles Times and later wrote for the Los Angeles Daily News.

Is two weeks by Karen Kingsbury part of a series?

From #1 New York Times bestselling author Karen Kingsbury comes a heart-wrenching and redemptive new story in the Baxter Family series about a couple desperately waiting to bring their adopted child home and a young mother about to make the biggest decision of her life.

Why does Alec have no teeth?

Alec is One in a Million

Alec was born with brittle bone disease, which means his bones can break very easily.

Do brittle bones cause pain?

There typically are no symptoms in the early stages of bone loss. But once your bones have been weakened by osteoporosis, you might have signs and symptoms that include: Back pain, caused by a fractured or collapsed vertebra. Loss of height over time.

Is osteoporosis a terminal illness?

Osteoporosis itself is not fatal. However, a fracture in the bone, particularly the hip, can have fatal outcomes, especially in women with osteoporosis. Hip fractures, even for patients with no bone disease take long to heal, and the period of immobility involved in healing can be longer for someone with osteoporosis.

What is van der Hoeve syndrome?

Van der Hoeve’s syndrome is the all-round variant of Lobstein’s disease (late osteogenesis imperfecta) and is characterized by the concurrent presence of osteoporosis, blue sclerae, and deafness. The literature has reported sporadic cases of a combination of algodystrophic syndrome and Lobstein’s disease.

Did Ivar the Boneless have osteogenesis imperfecta?

He was born with osteogenesis imperfecta, also known as brittle bone disease, a genetic disorder characterized by fragile bones that easily break (hence the name Ivar the Boneless). Due to this disease, Ivar is crippled and effectively ostracized from society.

Does osteogenesis imperfecta run in the family?

OI usually is inherited in a family in a pattern called autosomal dominant inheritance. Another way OI can be inherited is by autosomal recessive inheritance which is very rare. OI also can occur for the first time in a child of unaffected parents as a result of a new or “spontaneous” autosomal dominant mutation.

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