الملخص الإنجليزي
Ataxia telangiectasia (A-T) is a common, genetically inherited cause of early childhoodonset ataxia that is classically characterized by progressive cerebellar malfunction,
oculocutaneous telangiectasia, genome instability, and immunodeficiency. There is vast
phenotype variation in patients with A-T and recently, dystonia, an extrapyramidal
movement disorder. Here, we report the case of a 10-year-old girl who had experienced
repeated diarrhea and mild gait ataxia since the age of two years. At age seven, ataxia
and ocular telangiectasia were evident and immunoglobulin level assessment showed
hyper IgM immune phenotype, thus a diagnosis of A-T was made based on clinical
and laboratory findings, and she was started on intravenous immunoglobulin therapy.
Generalized dystonia appeared when she was 10-years-old. Molecular analysis revealed
two heterozygous mutations, c.6259delG and c.6658C>T, in the ATM gene of which
one (c.6259delG) is novel. Dystonia can be part of the clinical picture in the A-T disorder
and may even mask ataxia. This should be considered as a major feature mainly in variant
A-T, which may occur without general ataxia and may be misdiagnosed in adults with
primary dystonia.
