What are the symptoms of ataxia telangiectasia?

Many components. This is a recessive inherited disorder with many manifestations, most starting in early childhood including ataxic (drunken like) walking, peculiar eye tracking motions which inhibit learning, telangiectasia which are dilated blood vessels especially prominent on the eyes but also in sun exposed areas, and many other problems. Your pediatrician can help with diagnosis and management.

Related Questions

What is the relation between the nature and symptoms of xeroderma pigmentosum and ataxia telangiectasia?

Deficiency in some . part of cell mechanisms that detect & repair damage to DNA molecules that encode their genome occur in 5 inherited diseases: ataxia-telangiectasia (AT), Fanconi anemia, Bloom syndrome, Cockayne syndrome & Xeroderma Pigmentosum (XP).7 different mutant repair genes cause XP; types A, C, D & E are on Chromosome 9q.22. Mutations in ATM genes cause AT. Groups A,C,D & E are on Chromosome 11q2. . Read more...

What treats ataxia telangiectasia!?

Symptomatic. Ataxia telangiectasia is a genetic condition with no cure. As such, therapy is directed at treating consequences of this disease. For example, it is best to avoid excess radiation (excess x-rays, ct scans) be wary of any signs of infection (due to immune compromise) and be vigilant about signs of malignancy (weight loss, night sweats, etc.). Physical therapy is also recommended for ataxia. Read more...

What is the cure of ataxia telangiectasia?

Unfortunately none. Unfortunately there is no cure for ataxia telangiectasia. The only treatment is physical and occupational therapy to help maintain function that remain as the disease progresses. Read more...

Questions on ataxia telangiectasia causes?

Genetic. Ataxia telangiectasia is caused by a genetic mutation. It is transmitted in an autosomal recessive fashion. This means that for a child to get the disorder, they need to get one damaged chromosome from both parents. Because the parents only had one damaged chromosome, they are not affected; however, the child with two damaged chromosomes, will show signs of the disease. Read more...

What sort of problem is ataxia telangiectasia?

Ataxia. Ataxia telangiectasia is a condition in which abnormal vessel growth occurs in various parts of the body, especially in the motor control portion of the brain base (causing ataxia) and other parts of the body including the retina, kidney and other internal organs. It needs careful following by your physician with neurologic input at times. Read more...

Please tell me what causes ataxia telangiectasia!?

Genetic disorder. Louis–bar syndrome) is a rare, neurodegenerative, inherited disease causing severe disability. Ataxia refers to poor coordination and telangiectasia to small dilated blood vessels. A-t is caused by a defect in the atm gene, causing the gradual difficulty in coordination in walking, eye movements, etc. Read more...

Does anyone know of any good sites for information about ataxia telangiectasia?

Try these. I would refer to the national institute of health page at: http://www.Ninds.Nih.Gov/disorders/a_t/a-t.Htm as well as the national cancer institutes site at http://www.Cancer.Gov/cancertopics/factsheet/risk/ataxia these sites document frequent causes of morbidity in at, notably the ataxia as well as susceptibility to malignancy and immunocompromise that occur in this condition. Read more...

What is the treatment for ataxia telangiectasia?

Symptomatic. Ataxia telangiectasia is a genetic condition with no cure. As such, therapy is directed at treating consequences of this disease. For example, it is best to avoid excess radiation (excess x-rays, ct scans) be wary of any signs of infection (due to immune compromise) and be vigilant about signs of malignancy (weight loss, night sweats, etc.). Physical therapy is also recommended for ataxia. Read more...