Literature DB >> 18413472

Abnormal nerve conduction features in fragile X premutation carriers.

Kultida Soontarapornchai1, Ricardo Maselli, Grace Fenton-Farrell, Flora Tassone, Paul J Hagerman, Davis Hessl, Randi J Hagerman.   

Abstract

BACKGROUND: Distal neuropathy is part of the clinical phenotype in most males with the fragile X-associated tremor/ataxia syndrome (FXTAS) caused by the 55 to 200 CGG repeat expansion.
METHODS: We performed nerve conduction studies in 16 male carriers with FXTAS, 11 non-FXTAS carriers, and 11 control subjects and assessed the outcomes with respect to the fragile X mental retardation 1 genotype (FMR1) (Online Mendelian Inheritance in Man [OMIM] 309550; NT011681) and messenger RNA expression.
RESULTS: Men with FXTAS had slower tibial nerve conduction velocities and prolonged F-wave latencies compared with controls (z = 2.06, P = .04; and z = 2.73, P = .005) and unaffected premutation males (z = 1.98, P = .04; and z = 2.00, P = .04). Compound muscle action potential amplitudes were smaller in the FXTAS group relative to controls. Sural nerve action potential amplitudes were reduced in the FXTAS group compared with controls. After controlling for age, there was a significant relationship between the longer CGG repeat number and tibial nerve conduction velocity slowing (r = -0.42, P = .04) and between elevated messenger RNA levels and reduction of the tibial compound muscle action potential velocity (r = -0.52, P = .01) in the permutation group.
CONCLUSIONS: Male premutation carriers had significant conduction abnormalities of motor and sensory nerves that correlated with molecular measures, suggesting that the premutation FMR1 genotype is a causal factor. There was also evidence of nerve conduction abnormalities in non-FXTAS carriers compared with controls, which suggests that the neuropathy can occur without the full clinical presentation of FXTAS.

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Year:  2008        PMID: 18413472      PMCID: PMC2888466          DOI: 10.1001/archneur.65.4.495

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  16 in total

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Journal:  Neuromuscul Disord       Date:  2003-01       Impact factor: 4.296

2.  Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

Authors:  R J Hagerman; M Leehey; W Heinrichs; F Tassone; R Wilson; J Hills; J Grigsby; B Gage; P J Hagerman
Journal:  Neurology       Date:  2001-07-10       Impact factor: 9.910

3.  Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

Authors:  F Tassone; R J Hagerman; A K Taylor; L W Gane; T E Godfrey; P J Hagerman
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

4.  Phenotypic involvement in females with the FMR1 gene mutation.

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5.  Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.

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  38 in total

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3.  Small fiber neuropathy in a woman with fragile X-associated tremor/ataxia syndrome (FXTAS).

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4.  Late Onset Tremor and Ataxia Syndrome: FXTAS and its Ignored Peripheral Nervous System Findings in Diagnostic Criteria.

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Review 5.  Advances in understanding the molecular basis of FXTAS.

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Journal:  Hum Mol Genet       Date:  2010-04-29       Impact factor: 6.150

Review 6.  Fragile X-associated tremor/ataxia syndrome.

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Review 7.  Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management.

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Review 8.  [Fragile X-associated tremor/ataxia syndrome].

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9.  Prevalence and risk of migraine headaches in adult fragile X premutation carriers.

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