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Article in English | MEDLINE | ID: mdl-31565539

ABSTRACT

Background: Dystonia is a relatively common feature of spinocerebellar ataxia 3 (SCA3). Childhood onset of SCA3 is rare and typically associated with either relatively large, or homozygous, CAG repeat expansions. Case report: We describe a 10-year-old girl with SCA3, who presented with tongue dystonia in addition to limb dystonia and gait ataxia due to a heterozygous expansion of 84 repeats in ATXN3. Discussion: Diagnosis of the SCAs can be challenging, and even more so in children. Tongue dystonia has not previously been documented in SCA3.


Subject(s)
Dystonia/physiopathology , Gait Disorders, Neurologic/physiopathology , Machado-Joseph Disease/physiopathology , Tongue/physiopathology , Age of Onset , Ataxin-3/genetics , Child , Dystonia/etiology , Female , Gait Disorders, Neurologic/etiology , Humans , Machado-Joseph Disease/complications , Machado-Joseph Disease/genetics , Repressor Proteins/genetics , Trinucleotide Repeat Expansion/genetics
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