2013
DOI: 10.1055/s-0033-1337697
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Case report: oculomotor apraxia in ataxia telangiectasia

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Cited by 6 publications
(1 citation statement)
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“…Ataxia-telangiectasia (A-T) is a genetic neurodegenerative disorder described by several problems such as ataxia, telangiectasia, failure in motor ability, unusual eye movement, immunodeficiency, pulmonary disorder, and susceptibility to recurrent infections due to the mutation in the ATM gene on the chromosome 11q22.23. 1,2,11 These clinical complications play indispensable role in the morbidity and mortality of the disease. 6 In the present study, we investigated a child with A-T who had recurrent hospital admission due to repetitive infections, hematologic disorders, and neurological problems.…”
Section: Discussionmentioning
confidence: 99%
“…Ataxia-telangiectasia (A-T) is a genetic neurodegenerative disorder described by several problems such as ataxia, telangiectasia, failure in motor ability, unusual eye movement, immunodeficiency, pulmonary disorder, and susceptibility to recurrent infections due to the mutation in the ATM gene on the chromosome 11q22.23. 1,2,11 These clinical complications play indispensable role in the morbidity and mortality of the disease. 6 In the present study, we investigated a child with A-T who had recurrent hospital admission due to repetitive infections, hematologic disorders, and neurological problems.…”
Section: Discussionmentioning
confidence: 99%