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

36 Citations (Scopus)

Abstract

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. We describe 3 patients with FMR1 gray zone alleles who meet diagnostic criteria for FXTAS. 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)296-300
Number of pages5
JournalMovement disorders : official journal of the Movement Disorder Society
Volume27
Issue number2
StatePublished - Feb 2012

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

ASJC Scopus subject areas

  • Medicine(all)

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 : official journal of the Movement Disorder Society, Vol. 27, No. 2, 02.2012, p. 296-300.

Research output: Contribution to journalArticle

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