Fragile X Associated Tremor ataxia syndrome in FMR1 gray zone allele carriers

Deborah Hall, Flora Tassone, Olga Klepitskaya, Maureen Leehey

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Background: Carriers of fragile X mental retardation 1 (FMR1) repeat expansions in the premutation range (55-200 CGG repeats) often develop a syndrome of kinetic tremor, cerebellar ataxia, and parkinsonism; designated the fragile X-associated tremor ataxia syndrome (FXTAS). Neurological signs have not been reported in carriers of gray zone (45-54 CGG repeats) expansions. Methods/Results: We describe 3 patients with FMR1 gray zone alleles who meet diagnostic criteria for FXTAS. Conclusions: Our cases suggest that the definition of the FXTAS may need to be broadened to include individuals with FMR1 repeat expansions in the gray zone. These neurological signs may be due to elevated levels of expanded CGG repeat FMR1 mRNA in the gray zone carriers, similar to the changes seen in premutation carriers with FXTAS.

Original languageEnglish (US)
Pages (from-to)297-301
Number of pages5
JournalMovement Disorders
Volume27
Issue number2
DOIs
StatePublished - Feb 2012

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Intellectual Disability
Alleles
Cerebellar Ataxia
Parkinsonian Disorders
Tremor
Messenger RNA
Fragile X Tremor Ataxia Syndrome

Keywords

  • Ataxia
  • FMR1
  • FXTAS
  • Genetics
  • Gray zone

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Fragile X Associated Tremor ataxia syndrome in FMR1 gray zone allele carriers. / Hall, Deborah; Tassone, Flora; Klepitskaya, Olga; Leehey, Maureen.

In: Movement Disorders, Vol. 27, No. 2, 02.2012, p. 297-301.

Research output: Contribution to journalArticle

Hall, Deborah ; Tassone, Flora ; Klepitskaya, Olga ; Leehey, Maureen. / Fragile X Associated Tremor ataxia syndrome in FMR1 gray zone allele carriers. In: Movement Disorders. 2012 ; Vol. 27, No. 2. pp. 297-301.
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