Fibromyalgia in fragile X mental retardation 1 gene premutation carriers.

doi:10.1093/rheumatology/ker273

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Fibromyalgia in fragile X mental retardation 1 gene premutation carriers.

Rheumatology (Oxford, England) - 1 Dec 2011

Leehey Maureen A, Legg Wendi, Tassone Flora, Hagerman Randi

Abstract excerpt

OBJECTIVE: FM is a disorder of altered pain regulation and is characterized by pain, fatigue, poor sleep and psychological impairments; thus, it is classified as a central sensitivity syndrome. Female carriers of a premutation in the fragile X mental retardation 1 (FMR1) gene frequently have widespread musculoskeletal pain and sometimes have been diagnosed with FM, especially if they have the motor signs of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Fibromyalgia
Share to Fragile X Mental Retardation Protein
Share to Fragile X Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to FMR1 gene

Share to Heterozygote

Share to Mutation

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 21926154
DOI: 10.1093/rheumatology/ker273
PMCID: PMC3222847

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.