Meeting Abstracts of the 1st Fragile X International Congress

The aim of this Congress was to bring together clinicians and researchers working in the area of Fragile X Syndrome (FXS) and Fragile X Premutation Associated Conditions (FXPAC) from around the world, giving them the opportunity to network, be informed of the latest research from colleagues, workshop ideas through panel discussions, discuss translational research with clinical applications, and form relationships of future collaboration.The speakers' presentations covered various FMR1 premutation issues, biomarkers, behavioural aspects, treatment of FXS, mosaicism, models of care and expert centres in various countries, and more.A recently published paper, 'A Holis tic Appro ach to Fragi le X Syndr ome' , was presented and provides the reader with an overview of the scope of the Congress.

Institutions

Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2025-04-24
DOI
https://doi.org/10.1186/s13023-025-03574-x
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
0.00

Funders

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article

Meeting Abstracts of the 1st Fragile X International Congress

Orphanet Journal of Rare Diseases
Genetics and Neurodevelopmental Disorders
article

Meeting Abstracts of the 1st Fragile X International Congress

article en

Abstract

The aim of this Congress was to bring together clinicians and researchers working in the area of Fragile X Syndrome (FXS) and Fragile X Premutation Associated Conditions (FXPAC) from around the world, giving them the opportunity to network, be informed of the latest research from colleagues, workshop ideas through panel discussions, discuss translational research with clinical applications, and form relationships of future collaboration.The speakers' presentations covered various FMR1 premutation issues, biomarkers, behavioural aspects, treatment of FXS, mosaicism, models of care and expert centres in various countries, and more.A recently published paper, 'A Holis tic Appro ach to Fragi le X Syndr ome' , was presented and provides the reader with an overview of the scope of the Congress.

Orphanet Journal of Rare DiseasesVol. 20(S1)
Fidelity Investments (United States) (US)
Children’s Hospital of Wisconsin Research Institute, UK Research and Innovation, Murdoch Children's Research Institute, Australian Government, European Commission, University of Technology Sydney, Monash University, University of Adelaide, Economic and Social Research Council, Instituto de Salud Carlos III
Partnerships for the goals
Openalex Percentile: Top 90%
Genetics and Neurodevelopmental Disorders
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Meeting Abstracts of the 1st Fragile X International Congress · Orphanet Journal of Rare Diseases (2025) | TGRS Research Map | TGRS