Ataxia telangiectasia (patient information): Difference between revisions
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'''For the WikiDoc page for this topic, click [[Ataxia telangiectasia|here]]''' | '''For the WikiDoc page for this topic, click [[Ataxia telangiectasia|here]]''' | ||
{{Ataxia telangiectasia (patient information)}} | {{Ataxia telangiectasia (patient information)}} | ||
'''Editor-in-Chief:''' [[C. Michael Gibson]], M.S.,M.D. [mailto: | '''Editor-in-Chief:''' [[C. Michael Gibson]], M.S.,M.D. [mailto:charlesmichaelgibson@gmail.com] Phone:617-632-7753; '''Associate Editor-In-Chief:''' [[Varun Kumar]], M.B.B.S. | ||
==Overview== | ==Overview== | ||
*Ataxia-telangiectasia is rare childhood disease that affects the brain and other parts of the body. | *Ataxia-telangiectasia is rare childhood disease that affects the brain and other parts of the body. | ||
*[[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. | *[[Ataxia (patient information)|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. | ||
==What are the symptoms of Ataxia telangiectasia?== | ==What are the symptoms of Ataxia telangiectasia?== | ||
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:*Genetic testing to look for mutations in the ATM gene | :*Genetic testing to look for mutations in the ATM gene | ||
:*[[Glucose tolerance test]] | :*[[Glucose tolerance test]] | ||
:*Serum immunoglobulin levels (IgE, IgA) | :*Serum immunoglobulin levels ([[IgE]], [[IgA]]) | ||
:*X-rays to look at the size of the thymus gland | :*X-rays to look at the size of the [[thymus]] gland | ||
==Treatment options== | ==Treatment options== | ||
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{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:For review]] | [[Category:For review]] | ||
[[Category:Overview complete]] | [[Category:Overview complete]] | ||
[[Category:Template complete]] | [[Category:Template complete]] | ||
[[Category:Disease | [[Category:Disease]] | ||
[[Category:Patient information]] | [[Category:Patient information]] | ||
[[Category:Neurology]] | [[Category:Neurology]] | ||
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[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
[[Category:Pediatrics patient information]] | [[Category:Pediatrics patient information]] | ||
Latest revision as of 15:00, 29 November 2012
For the WikiDoc page for this topic, click here
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Ataxia telangiectasia |
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Ataxia telangiectasia On the Web |
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Editor-in-Chief: C. Michael Gibson, M.S.,M.D. [1] Phone:617-632-7753; Associate Editor-In-Chief: Varun Kumar, M.B.B.S.
Overview
- Ataxia-telangiectasia is rare childhood disease that affects the brain and other parts of the body.
- 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.
What are the symptoms of Ataxia telangiectasia?
- Decreased coordination of movements (ataxia) in late childhood
- Ataxic gait (cerebellar ataxia)
- Jerky gait
- Unsteady
- Decreasing mental development, slows or stops after age 10-12
- Delayed walking
- Discoloration of skin areas exposed to sunlight
- Discoloration of skin (coffee-with-milk colored spots)
- Enlarged blood vessels in skin of nose, ears, and inside of the elbow and knee
- Enlarged blood vessels in the whites of the eyes
- Jerky or abnormal eye movements (nystagmus) late in the disease
- Premature graying of the hair
- Seizures
- Sensitivity to radiation, including medical x-rays
- Severe respiratory infections that keep coming back (recurring)
What causes Ataxia telangiectasia?
- Ataxia-telangiectasia is inherited, which means it is passed down through families. It is an autosomal recessive trait. This means that both parents must provide a defective gene for the child to have symptoms of the disorder.
- The disease results from defects in the ataxia telangiectasia mutated (ATM) gene. Defects in this gene can lead to abnormal cell death in various places of the body, including the part of the brain that helps coordinate movement.
- Boys and girls are equally affected.
When to seek urgent medical care?
Call your health care provider if your child develops symptoms of this disorder.
Diagnosis
- The doctor will perform a physical exam. Examination may show signs of the following:
- Below normal sized tonsils, lymph nodes, and spleen
- Decreased-to-absent deep tendon reflexes
- Delayed or absent physical and sexual development
- Growth failure
- Mask-like face
- Multiple skin coloring and texture changes
- Possible tests include:
- Alpha fetoprotein
- B and T cell screen
- Carcinoembryonic antigen
- Genetic testing to look for mutations in the ATM gene
- Glucose tolerance test
- Serum immunoglobulin levels (IgE, IgA)
- X-rays to look at the size of the thymus gland
Treatment options
- There is no specific treatment for ataxia-telangiectasia.
- Treatment is directed at specific symptoms.
Where to find medical care for Ataxia telangiectasia?
Directions to Hospitals Treating Ataxia telangiectasia
What to expect (Outlook/Prognosis)?
- Early death is common, but life expectancy varies.
- Because persons with this condition are very sensitive to radiation, they should never be given radiation therapy, and no unnecessary x-rays should be done.
Possible complications
- Cancer such as lymphoma
- Diabetes
- Kyphosis
- Progressive movement disorder that leads to wheelchair use
- Scoliosis
- Severe, recurrent lung infections
Prevention
- Couples with a family history of this condition who are considering pregnancy may consider genetic counseling.
- Parents of a child with this disorder may have a slight increased risk of cancer. They should have genetic counseling and more intensive cancer screenings.