Is ataxia telangiectasia a cancer?

What is the life expectancy of someone with ataxia telangiectasia?

Ataxia telangiectasia is a rare, multiorgan neurodegenerative disorder with enhanced vulnerability to cancer and infection. Median survival in two large cohorts of patients with this disease, one prospective and one retrospective, is 25 and 19 years, with a wide range.

How do people get ataxia telangiectasia?

Ataxia telangiectasia is inherited as an autosomal recessive trait. Genetic diseases are determined by two genes, one received from the father and one from the mother. Recessive genetic disorders occur when an individual inherits the same abnormal gene for the same trait from each parent.

What body systems are affected by ataxia telangiectasia?

Ataxia-telangiectasia (AT) is a rare inherited condition that affects the nervous system, the immune system and other body systems. It is characterized by the presence of: Progressive ataxia (lack of coordination) due to a defect in the cerebellum (the part of the brain involved in coordinating the movement of muscles)

Can ataxia telangiectasia be cured?

General Treatment of Ataxia-Telangiectasia. There is no cure for any of the problems associated with A-T. Treatment is supportive but should be proactive.

Can ataxia be cured?

There’s no treatment specifically for ataxia. In some cases, treating the underlying cause resolves the ataxia, such as stopping medications that cause it. In other cases, such as ataxia that results from chickenpox or other viral infections, it’s likely to resolve on its own.

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How do you prevent ataxia telangiectasia?


  1. Physical Therapy. Studies show that the single most important supportive therapy for A-T patients is aggressive physical therapy (Spacey et al. …
  2. Intravenous Immunoglobulin (IVIG) Treatment. …
  3. Radiation Avoidance. …
  4. Breast Cancer Screening.

Can people with ataxia telangiectasia have children?

The parents of a child with ataxia-telangiectasia have a 25% (1 in 4) chance of having another child with the condition. They have a 50% (1 in 2) chance of having a child who carries just one copy of an ATM mutation. That child would be a carrier.

Is Ataxia a rare disease?

Ataxia usually develops as a result of damage to a part of the brain that coordinates movement (cerebellum). Ataxia can develop at any age. It is typically progressive, meaning it can get worse with time. It is a rare condition, affecting about 150,000 people in the U.S.

What does ataxia telangiectasia look like?

Ataxia refers to uncoordinated movements, such as walking. Telangiectasias are enlarged blood vessels (capillaries) just below the surface of the skin. Telangiectasias appear as tiny, red, spider-like veins.