Add to ORKGFragile X syndrome (FXS), the most common inherited cause of intellectual disability, learning disability, and autism spectrum disorder, is associated with an increased prevalence of certain medical conditions including seizures. The goal of this study was to better understand seizures in individuals with FXS using the Fragile X Online Registry with Accessible Research Database, a multisite observational study initiated in 2012 involving FXS clinics in the Fragile X Clinic and Research Consortium. Seizure data were available for 1,607 participants, mostly male (77%) and white (74.5%). The overall prevalence of at least one seizure was 12%, with this rate being significantly higher in males than females (13.7 vs. 6.2%
Background: Fragile X Syndrome (FXS) is the second cause of intellectual disability after Down syndr...
Funding Information: The study was approved by the Latvian Central Medical Ethics Committee and the ...
Fragile X syndrome (FXS) is the most common single gene cause of intellectual disability and autism ...
Fragile X syndrome (FXS), the most common inherited cause of intellectual disability, learning disab...
BackgroundFragile X syndrome is characterized by a myriad of physical features, behavioral features,...
BACKGROUND: Fragile X syndrome (FXS), caused by a mutation of the FMR1 gene on the X chromosome, is ...
Background: Fragile X Syndrome (FXS) is the second cause of intellectual disability after Down syndr...
Fragile X syndrome (FXS) is the most common cause of inherited intellectual disability and a variant...
BACKGROUND AND OBJECTIVEIndividuals with fragile X syndrome (FXS) are frequently codiagnosed with au...
Summary: Purpose and Methods: One hundred and ninetytwo fragile X male patients were investigated f...
ObjectiveThe phenotypic impact of fragile X syndrome (FXS) has been well-documented since the discov...
Fragile X Syndrome (FXS) is the most common cause of inherited intellectual disability with prevalen...
Background As data on the phenotype, characteristics and management of patients with Fragile X Syndr...
RATIONALE: Advances in understanding the underlying mechanisms of conditions such as fragile X syndr...
Fragile X syndrome (FXS) is caused by the full mutation (>200 CGG repeats) in the Fragile X Menta...
Background: Fragile X Syndrome (FXS) is the second cause of intellectual disability after Down syndr...
Funding Information: The study was approved by the Latvian Central Medical Ethics Committee and the ...
Fragile X syndrome (FXS) is the most common single gene cause of intellectual disability and autism ...
Fragile X syndrome (FXS), the most common inherited cause of intellectual disability, learning disab...
BackgroundFragile X syndrome is characterized by a myriad of physical features, behavioral features,...
BACKGROUND: Fragile X syndrome (FXS), caused by a mutation of the FMR1 gene on the X chromosome, is ...
Background: Fragile X Syndrome (FXS) is the second cause of intellectual disability after Down syndr...
Fragile X syndrome (FXS) is the most common cause of inherited intellectual disability and a variant...
BACKGROUND AND OBJECTIVEIndividuals with fragile X syndrome (FXS) are frequently codiagnosed with au...
Summary: Purpose and Methods: One hundred and ninetytwo fragile X male patients were investigated f...
ObjectiveThe phenotypic impact of fragile X syndrome (FXS) has been well-documented since the discov...
Fragile X Syndrome (FXS) is the most common cause of inherited intellectual disability with prevalen...
Background As data on the phenotype, characteristics and management of patients with Fragile X Syndr...
RATIONALE: Advances in understanding the underlying mechanisms of conditions such as fragile X syndr...
Fragile X syndrome (FXS) is caused by the full mutation (>200 CGG repeats) in the Fragile X Menta...
Background: Fragile X Syndrome (FXS) is the second cause of intellectual disability after Down syndr...
Funding Information: The study was approved by the Latvian Central Medical Ethics Committee and the ...
Fragile X syndrome (FXS) is the most common single gene cause of intellectual disability and autism ...
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