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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.

Surprising Molecular Pattern in Fragile X Syndrome Revealed

Surprising Molecular Pattern in Fragile X Syndrome Revealed

Fragile X Syndrome is linked to significant DNA misfolding leading to gene silencing, affecting synaptic and connective tissues.

PARMESAN: New AI Tool Revolutionizing Genetic Disorder Treatments

PARMESAN: New AI Tool Revolutionizing Genetic Disorder Treatments

PARMESAN, the natural language processing tool accelerates research, boosting drug discovery and development for scientists.

Fragile X Syndrome Treatment Will be Changed by 2030

Fragile X Syndrome Treatment Will be Changed by 2030

The leading data analytics company notes that pipeline drugs will help propel the Fragile X syndrome (FXS) market and will add $23.3 million to the market by 2030.

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Repurposed Amyotrophic Lateral Sclerosis (ALS) Drug Against Rare Genetic Disorder

Repurposed Amyotrophic Lateral Sclerosis (ALS) Drug Against Rare Genetic Disorder

Repurposed ALS (amyotrophic lateral sclerosis) drug may help slow down a rare genetic disorder in children and adolescents.

New Genetic Disorder Affects Brain and Craniofacial Skeleton

New Genetic Disorder Affects Brain and Craniofacial Skeleton

Researchers at the National Institutes of Health have discovered a new genetic disorder characterized by developmental delays and malformations of the brain, heart and facial features.

Link Between Fragile X Syndrome and the Fetal Brain

Link Between Fragile X Syndrome and the Fetal Brain

New study has offered fresh insights into the fetal development of our brain and the potential causes of Fragile X syndrome (FSX).

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FDA Approves the First Drug to Treat an Rare Genetic Disorder Which Causes Kidney Stones

FDA Approves the First Drug to Treat an Rare Genetic Disorder Which Causes Kidney Stones

FDA has approved lumasiran subcutaneous injection to treat adults and children with primary hyperoxaluria type 1 (PH1)- an ultra- rare genetic disorder.

New Treatment Benefits Patients With Rare Genetic Disorder

New Treatment Benefits Patients With Rare Genetic Disorder

In patients with rare genetic disorder, existing drugs were found to improve neurological function, revealed new study.

Fragile X Syndrome Treatment: New Insights

Fragile X Syndrome Treatment: New Insights

Scientists are working globally to educate clinicians and families on how to identify, test and provide care for those born with fragile X syndrome, often linked to autism.

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Milk or No Milk for Babies With a Rare Type of Genetic Disorder

Milk or No Milk for Babies With a Rare Type of Genetic Disorder

The study found that children with Duarte galactosemia are at no greater risk of long-term developmental abnormalities than their unaffected siblings, with exposure to milk as infants.

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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.