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Fragile X Syndrome News, Research and Latest Updates

Keep abreast with the latest news related to Fragile X Syndrome there are 78 news items on Fragile X Syndrome that covers updates, breakthroughs and in-depth reports.

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Fragile X Syndrome

Fragile X syndrome is an inherited X-linked genetic disorder that results in developmental and intellectual disabilities, along with behavioral problems.

Fragile X Syndrome Linked to Autism

Fragile X Syndrome Linked to Autism

For many years, doctors have known that patients with fragile X syndrome, the most common form of inherited intellectual disability, are often also diagnosed with autism.

Genetic Disorder In Children Linked To Poor Adaptive Behavior

Genetic Disorder In Children Linked To Poor Adaptive Behavior

UC Davis researchers have found that for children with the genetic disorder known as chromosome 22q11.2 deletion syndrome anxiety is linked to poorer adaptive behaviors.

Rare Genetic Disorder Points to Molecular Pathway Linked to Schizophrenia

Rare Genetic Disorder Points to Molecular Pathway Linked to Schizophrenia

Scientists exploring a genetic disorder have discovered a molecular pathway that may play a role in schizophrenia, and perhaps lead to new treatment options for people with schizophrenia.

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Increasing Natural Marijuana-like Brain Chemicals Possible Treatment for Fragile X Syndrome Symptoms

Increasing Natural Marijuana-like Brain Chemicals Possible Treatment for Fragile X Syndrome Symptoms

Boosting natural marijuana-like chemicals in the brain can help correct behavioral issues related to fragile X syndrome, the most common known genetic cause of autism.

Genetic Disorder is Passed on to Five Children by the Sperm Donor

Genetic Disorder is Passed on to Five Children by the Sperm Donor

After a screening test failed to catch that a Danish sperm donor had the disease,he has potentially passed a severe genetic disorder to five children.

Rare Genetic Disorder can be Studied in New Mouse Model

Rare Genetic Disorder can be Studied in New Mouse Model

Researchers can utilize new mouse models to study a rare genetic disorder known as SECISBP2 syndrome

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New Mouse Model may Provide Insights into Severe Genetic Disorder in Children

New Mouse Model may Provide Insights into Severe Genetic Disorder in Children

New mouse models can help researchers study MCT8 deficiency - an inherited genetic disorder in children, says study. MCT8 deficiency is a serious diagnosis.

Novel Compound Holds Promise for Treating Genetic Disorders in Muscles

Novel Compound Holds Promise for Treating Genetic Disorders in Muscles

A new compound holds promise for treating Duchenne muscular dystrophy and other inherited disorders.

Fresh Insight on Rare Genetic Disorders That Impair Childhood Growth and Development

Fresh Insight on Rare Genetic Disorders That Impair Childhood Growth and Development

Research on rare genetic disorders has opened up fresh insights into those diseases in biological structures that regulate chromosomes when cells divide.

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New Compound Reverses Fragile X Syndrome Symptoms

New Compound Reverses Fragile X Syndrome Symptoms

A novel compound reverses many of the major symptoms associated with Fragile X Syndrome (FXS), say scientists.

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Ehlers-Danlos syndrome: Symptoms Diagnosis Treatment

Ehlers-Danlos syndrome: Symptoms Diagnosis Treatment

Ehlers-Danlos syndrome is a group of inherited disorders that affect the connective tissues of the skin, joints and walls of the blood vessels. It is characterized by flexible joints and fragile skin.