Ataxia-telangiectasia Presenting with Craniostenosis

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Ataxia-telangiectasia presenting with craniostenosis.

Ataxia-telangiectasia is a familial syndrome which gradually unfolds during early childhood. It is characterized by progressive cerebellar ataxia, symmetrical telangiectasia, frequent respiratory infections, delayed physical but normal mental development and quite often a dry skin with cafe-au-lait spots. The first published case by Louis-Bar (1941) was followed by fuller and welldocumented rep...

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Dystonia as presenting manifestation of ataxia telangiectasia : a case report.

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Ataxia-telangiectasia

Objective Ataxia-telangiectasia (AT) is a rare, severe, and ineluctably progressive multisystemic neurodegenerative disease. Variant AT phenotypes have been described in patients with mildand late-onset neurologic deterioration and atypical features (dystonia and myoclonus). We report on the clinical characteristics and transcriptome profile of patients with a typical AT presentation and genoty...

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Ataxia-telangiectasia is a complex syndrome that includes a very high cancer risk in children with a progressive cerebellar ataxia, the onset of which occurs in early infancy. Ocular telangiectasiae often do not appear until several years after the ataxia. The most common type of malignancy is lymphoma, usually of the B-cell type. Leukemias also occur. Failure to diagnose ataxia-telangiectasia ...

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Onset of the disease is often during the second year of life: there is progressive cerebellar ataxia (initially truncal, with further peripheral extend); ataxia is a constant feature in this disease; oculomotor apraxia, dysarthria, and dystonia; leading to muscular atrophia. Telangiectasia: facial region exposed to sunlight, and eyes (conjunctiva). Combined immunodeficiency (in 70 %): thymus hy...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1962

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.37.196.652