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Down Syndrome News, Research and Latest Updates

Keep abreast with the latest news related to Down Syndrome there are 191 news items on Down Syndrome that covers updates, breakthroughs and in-depth reports.

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Down Syndrome

Down Syndrome is a congenital disorder among children commonly born to older mothers. The condition is also known as ‘Up syndrome’ because of the cheerful persona of the Down children.

Neurodevelopmental Treatment for Kids With Down Syndrome

Neurodevelopmental Treatment for Kids With Down Syndrome

World Down Syndrome Day: 2024 theme "End The Stereotypes," emphasizes the importance of inclusivity and discourages discrimination against individuals with Down syndrome.

End the Stereotypes: World Down Syndrome Day

End the Stereotypes: World Down Syndrome Day

Challenging misconceptions, embracing diversity, and advocating for inclusion for individuals with Down syndrome.

Snhg11 Gene: Key to Down Syndrome Memory & Cognitive Deficits

Snhg11 Gene: Key to Down Syndrome Memory & Cognitive Deficits

Discover the pivotal role of the Snhg11 gene in hippocampal neuron function and memory formation, providing insights on Down syndrome cognitive impairments.

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Gene Dyrk1a Linked to Heart Defects in Down Syndrome Identified

Gene Dyrk1a Linked to Heart Defects in Down Syndrome Identified

In Down syndrome patients, partially mitigating the overactivity of the Dyrk1a gene in mice reversed the defects laying the groundwork for potential future therapies.

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.

How Can Caregivers Best Address Gynecological Needs in Down Syndrome Women?

How Can Caregivers Best Address Gynecological Needs in Down Syndrome Women?

The study's results provide valuable insights into the gynecological care needs of young girls and women with Down syndrome.

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Genetic Basis of Facial Changes in Down Syndrome Revealed

Genetic Basis of Facial Changes in Down Syndrome Revealed

In Down Syndrome condition, mouse strains with duplications of three regions on chromosome 16, which mirrors having a third chromosome 21 have been created.

Gene In Down Syndrome Patients Stops Other Neurons’ Action

Gene In Down Syndrome Patients Stops Other Neurons’ Action

The gene present in an extra copy of human chromosome 21 that causes Down syndrome could be responsible for neurological disorder symptoms.

Is Diabetes More Common Among Kids With Down Syndrome

Is Diabetes More Common Among Kids With Down Syndrome

Diabetes and obesity are more common among children and young adults with Down Syndrome.

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Down Syndrome Patients Face Problems With Fracture Healing

Down Syndrome Patients Face Problems With Fracture Healing

Fracture healing in patients with Down syndrome is a major concern. They may not heal completely.

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Recommended Reading

A Special Day With Down Syndrome

A Special Day With Down Syndrome

Time spent at the day care centre of the Down's Syndrome Association of India can be a lesson in humility and gratitude.

Birth Defect - Genetic

Birth Defect - Genetic

Achondroplasia is a genetic disorder which is one of the leading causes of dwarfism

XY Females - Women or Men

XY Females - Women or Men

All hell broke loose for Semenya, the South African athlete when laboratory tests proved that she was more a male than a female.

Test your Knowledge on Down Syndrome

Test your Knowledge on Down Syndrome

Down syndrome also known as Trisomy 21 is a genetic disorder caused by the presence of a third copy of chromosome 21. Down syndrome leads to impairments in cognitive ability and physical growth of the ...

Infographics on Down Syndrome

Infographics on Down Syndrome

Down syndrome (DS) is a chromosomal disorder. Down syndrome Infographic captures all the key data you need to know about the Down syndrome

Top 10 Facts on Down Syndrome

Top 10 Facts on Down Syndrome

Here are some interesting facts on Down syndrome or trisomy 21, where the affected children usually have an extra chromosome 21.

Hirschsprungs Disease

Hirschsprungs Disease

Hirschsprung disease is a type of functional bowel obstruction due to absence of nerves within the wall of a part of the large intestine in babies.

Exotropia or outward eye deviation is a form of squint. Proper evaluation and timely intervention is necessary to prevent permanent forms of visual dysfunction.