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Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006
See this aricle in Pubmed

Article Abstract
Genetic analysis of the FMR1 gene could provide a reliable diagnostic tool for the definitive diagnosis of late-onset ataxias. Additional studies are needed to clarify the importance of permutation screening in patients with movement disorders or other associated atypical features at onset, such as paraparesis.
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Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome,carrier
genetic testing
inclusion bodies
inclusion bodies,ubiquitin
middle cerebellar peduncle
middle cerebellar peduncle,lesion
molecular genetics
spinocerebellar ataxia
white matter disease

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