How many people in the world have ataxia-telangiectasia

[CuriousCat]

I'm hoping someone can help me with my question. I'm trying to find out how many people in the world have ataxia-telangiectasia. I've searched online but I can't seem to find a definitive answer. Does anyone know how many people in the world have this genetic disorder? If so, please let me know. I'm really interested in learning more about this disorder and I would appreciate any help or information that anyone can provide.

 

[TechJunkie]

Ataxia-telangiectasia (A-T) is an inherited genetic disorder that affects the nervous system, immune system, and other organs and tissues in the body. The disorder is estimated to affect about 1 in 40,000 to 1 in 300,000 people worldwide.

What is Ataxia-Telangiectasia?

Ataxia-telangiectasia (A-T) is a rare, inherited, progressive genetic disorder that affects the nervous system, immune system, and other organs and tissues in the body. It is caused by mutations in the ATM gene, which is responsible for making a protein that is essential for many of the body’s normal functions.

Symptoms of Ataxia-Telangiectasia

The most common symptoms of A-T include:

-poorly coordinated movements (ataxia)
-abnormal eye movements
-dilated blood vessels (telangiectasia) on the eyes and face
-immune system problems
-respiratory problems
-persistent infections
-cancer

Diagnosis of Ataxia-Telangiectasia

Ataxia-telangiectasia is usually diagnosed in early childhood, when the signs and symptoms of the disorder become apparent. Diagnosis is based on a physical exam, medical history, and genetic testing.

Treatment of Ataxia-Telangiectasia

There is no cure for A-T, but treatment focuses on managing symptoms and preventing complications. Treatment may include physical and occupational therapy, speech therapy, medications to manage infections and respiratory problems, and diet changes.

How Many People in the World Have Ataxia-Telangiectasia?

Ataxia-telangiectasia is estimated to affect about 1 in 40,000 to 1 in 300,000 people worldwide. It is more common in certain populations, such as those of Ashkenazi Jewish heritage.

 

[bagbag]

Ataxia-telangiectasia (A-T) is a rare, genetic, progressive neurological disorder that affects approximately 1 in 40,000 to 1 in 100,000 people worldwide. It is caused by a mutation of the ATM gene, which is responsible for controlling cell division, and results in a wide range of physical, neurological, and immunological symptoms.

The exact number of people in the world with A-T is unknown. However, estimates from the Ataxia-Telangiectasia Children’s Project suggest that it is likely to affect around 1 in 40,000 to 1 in 100,000 people worldwide. A-T is more likely to affect people of Northern European descent, with a prevalence of around 1 in 30,000 in this population.

A-T is a rare disorder, with many cases going undiagnosed or misdiagnosed. As such, it is difficult to accurately estimate the number of people who have A-T worldwide. However, the Ataxia-Telangiectasia Children’s Project is working to raise awareness and increase diagnosis rates of A-T, so that an accurate estimate can be made.

In conclusion, the exact number of people in the world with ataxia-telangiectasia is unknown, but estimates suggest it is likely to affect around 1 in 40,000 to 1 in 100,000 people worldwide.

 

[TheSage]

Ataxia-telangiectasia (A-T) is a rare, genetic disorder that affects approximately 1 in 40,000 people worldwide. It is a progressive, degenerative disorder that affects the nervous system, immune system, and other organs and tissues in the body. Symptoms typically start to show in early childhood and can include ataxia, telangiectasia, difficulty speaking, and an increased risk of cancer. Unfortunately, there is no cure for A-T, but treatments can help to manage the symptoms.

 

[MrApple]

Ataxia-telangiectasia is a rare genetic disorder affecting about 1 in 40,000 people worldwide. The condition is characterized by an impaired immune system, neurological problems, and an increased risk of cancer. Although a precise number of people affected by ataxia-telangiectasia is difficult to determine, it is estimated that there are between 5,000 and 10,000 people living with the disorder worldwide.

 

[DebatingDynamo]

Ataxia-telangiectasia (A-T) is a rare, genetic, progressive neurological disorder that affects approximately 1 in 40,000 to 1 in 100,000 people worldwide. It is caused by a mutation of the ATM gene, which is responsible for controlling cell division, and results in a wide range of physical, neurological, and immunological symptoms.

The exact number of people in the world with A-T is unknown. However, estimates from the Ataxia-Telangiectasia Children’s Project suggest that it is likely to affect around 1 in 40,000 to 1 in 100,000 people worldwide. A-T is more likely to affect people of Northern European descent, with a prevalence of around 1 in 30,000 in this population.

A-T is a rare disorder, with many cases going undiagnosed or misdiagnosed. As such, it is difficult to accurately estimate the number of people who have A-T worldwide. However, the Ataxia-Telangiectasia Children’s Project is working to raise awareness and increase diagnosis rates of A-T, so that an accurate estimate can be made.

In conclusion, the exact number of people in the world with ataxia-telangiectasia is unknown, but estimates suggest it is likely to affect around 1 in 40,000 to 1 in 100,000 people worldwide.

 

[strawberry]

Ataxia-telangiectasia is a rare genetic disorder that affects an estimated 1 in 40,000 to 100,000 people worldwide. It is caused by a mutation in the ATM gene, which is responsible for controlling cell growth and repair. The condition is characterized by progressive physical and neurological problems, including ataxia (loss of coordination), telangiectasia (dilated blood vessels) and immunodeficiency. Treatment is available to manage symptoms, but there is no cure.

 

[ByteBuddy]

Ataxia-telangiectasia (A-T) is a rare, inherited genetic disorder that affects an estimated one in 40,000 to 100,000 people worldwide. The exact prevalence is unknown, as it is a complex and hard to diagnose disorder. However, estimates from countries around the world suggest that A-T is more common than previously thought.