Rare Genetic Disorder
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Who Was Danny Go’s Son Isaac? YouTuber Announces Death of 14-Year-Old Son Due to Rare Genetic Condition
YouTube News: Danny Go, the popular children’s YouTuber, shared heartbreaking news about his 14-year-old son Isaac. Fans are now learning more about Isaac’s battle with Fanconi anemia and the emotional tribute posted by Danny.
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India Among Countries With Comprehensive National Rare Diseases Framework, Says Government
New Delhi, May 5 (IANS) The government on Tuesday said that the need for addressing rare diseases was first highlighted in the National Health Policy, 2017, and was subsequently institutionalized through the launch of the National Policy for Rare Dis
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How Scientists Changed Their View Of Insomnia
Insomnia rarely occurs on its own, which brings us to one of the biggest changes scientists have made in our understanding of chronic sleep deprivation.
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World Haemophilia Day 2026: Why Are Men More Likely To Develop Haemophilia?
On World Haemophilia Day 2026, Dr Rahul Bhargava explains why haemophilia affects men more than women. And understanding how the disorder can occur in your body, here is what you need to know about haemophilia.
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Understanding Hemophilia: Doctor Explains Symptoms, Treatment And Daily Challenges
Hemophilia is a rare genetic bleeding disorder affecting clotting ability. Here are its symptoms, treatment options, and everyday challenges, highlighting how early diagnosis, modern therapies, and lifestyle care can improve quality of life.
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DNA Mutations In Immune Cells May Be Driving Autoimmune Diseases, Study Finds
A new Nature study suggests DNA mutations in immune cells may drive autoimmune diseases by removing immune system brakes, offering clues for targeted treatments.
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Delhi Government's ANMOL Scheme To Boost Newborn Healthcare, Improve Emergency Response
After the launch of the ANMOL scheme to provide screening tests for genetic and metabolic disorders in newborns, medical experts say the scheme will drive early detection and help critical cases reach hospitals within the golden hour'.
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Nick Jonas' Friend Maya Kibbel Dies Of Wilson's Disease At 30: Signs And Risks Of The Rare Disease Explained
Nick Jonas lost his friend Maya Kibbel to Wilson's disease. Here is how the rare genetic disorder can manifest in the human body, along with the available treatment options.
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Nick Jonas's Childhood Friend Maya Kibbel Dies At 30, Singer Pays Tribute
Maya's mother described the difficult health battle her daughter had faced and the pain she endured during the course of the disease
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Researchers Uncover A Rare Form Of Diabetes In Newborns
A recent study has identified a genetic disorder that causes diabetes in some newborns. The study was published in The Journal of Clinical Investigation.
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The Invisible Disorder: An Indian Mother Shares How An Ultra-Rare Genetic Disease Reshaped Her Family's Life
Norrie Disease is an ultra-rare genetic disorder causing congenital blindness, progressive hearing loss and neurological challenges. One Indian mother's journey reveals how misunderstood the condition is, and why early genetic screening and awareness
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Did Adolf Hitler Really Have A Micropenis? Rare Genetic Disorder Kallmann Syndrome Explained
Kallmann Syndrome is a rare genetic disorder that causes delayed puberty and a poor sense of smell. New DNA findings suggest Adolf Hitler may have had features of this condition.
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"World Revolves Around...": DY Chandrachud Explains Why Moving Out Not Easy
The former Chief Justice has now spoken exclusively with NDTV about his daughters Priyanka and Mahi, who are in his foster care,
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Study Finds New Genetic Disorder Impacts Brain Development In Children
A team led by the University of Otago-Otakou Whakaihu Waka from New Zealand pinpointed specific changes in a gene called CRNKL1 that can potentially cause a severe genetic disorder with microcephaly and severe intellectual disability.
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Prince Frederik Of Luxembourg's Final Act Of Bravery Before Death At 22
Prince Frederik of Luxembourg was diagnosed with POLG mitochondrial disease, a rare genetic disorder affecting approximately one in 5,000 people, at the age of 14.
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Who Was Danny Go’s Son Isaac? YouTuber Announces Death of 14-Year-Old Son Due to Rare Genetic Condition
YouTube News: Danny Go, the popular children’s YouTuber, shared heartbreaking news about his 14-year-old son Isaac. Fans are now learning more about Isaac’s battle with Fanconi anemia and the emotional tribute posted by Danny.
-
India Among Countries With Comprehensive National Rare Diseases Framework, Says Government
New Delhi, May 5 (IANS) The government on Tuesday said that the need for addressing rare diseases was first highlighted in the National Health Policy, 2017, and was subsequently institutionalized through the launch of the National Policy for Rare Dis
-
How Scientists Changed Their View Of Insomnia
Insomnia rarely occurs on its own, which brings us to one of the biggest changes scientists have made in our understanding of chronic sleep deprivation.
-
World Haemophilia Day 2026: Why Are Men More Likely To Develop Haemophilia?
On World Haemophilia Day 2026, Dr Rahul Bhargava explains why haemophilia affects men more than women. And understanding how the disorder can occur in your body, here is what you need to know about haemophilia.
-
Understanding Hemophilia: Doctor Explains Symptoms, Treatment And Daily Challenges
Hemophilia is a rare genetic bleeding disorder affecting clotting ability. Here are its symptoms, treatment options, and everyday challenges, highlighting how early diagnosis, modern therapies, and lifestyle care can improve quality of life.
-
DNA Mutations In Immune Cells May Be Driving Autoimmune Diseases, Study Finds
A new Nature study suggests DNA mutations in immune cells may drive autoimmune diseases by removing immune system brakes, offering clues for targeted treatments.
-
Delhi Government's ANMOL Scheme To Boost Newborn Healthcare, Improve Emergency Response
After the launch of the ANMOL scheme to provide screening tests for genetic and metabolic disorders in newborns, medical experts say the scheme will drive early detection and help critical cases reach hospitals within the golden hour'.
-
Nick Jonas' Friend Maya Kibbel Dies Of Wilson's Disease At 30: Signs And Risks Of The Rare Disease Explained
Nick Jonas lost his friend Maya Kibbel to Wilson's disease. Here is how the rare genetic disorder can manifest in the human body, along with the available treatment options.
-
Nick Jonas's Childhood Friend Maya Kibbel Dies At 30, Singer Pays Tribute
Maya's mother described the difficult health battle her daughter had faced and the pain she endured during the course of the disease
-
Researchers Uncover A Rare Form Of Diabetes In Newborns
A recent study has identified a genetic disorder that causes diabetes in some newborns. The study was published in The Journal of Clinical Investigation.
-
The Invisible Disorder: An Indian Mother Shares How An Ultra-Rare Genetic Disease Reshaped Her Family's Life
Norrie Disease is an ultra-rare genetic disorder causing congenital blindness, progressive hearing loss and neurological challenges. One Indian mother's journey reveals how misunderstood the condition is, and why early genetic screening and awareness
-
Did Adolf Hitler Really Have A Micropenis? Rare Genetic Disorder Kallmann Syndrome Explained
Kallmann Syndrome is a rare genetic disorder that causes delayed puberty and a poor sense of smell. New DNA findings suggest Adolf Hitler may have had features of this condition.
-
"World Revolves Around...": DY Chandrachud Explains Why Moving Out Not Easy
The former Chief Justice has now spoken exclusively with NDTV about his daughters Priyanka and Mahi, who are in his foster care,
-
Study Finds New Genetic Disorder Impacts Brain Development In Children
A team led by the University of Otago-Otakou Whakaihu Waka from New Zealand pinpointed specific changes in a gene called CRNKL1 that can potentially cause a severe genetic disorder with microcephaly and severe intellectual disability.
-
Prince Frederik Of Luxembourg's Final Act Of Bravery Before Death At 22
Prince Frederik of Luxembourg was diagnosed with POLG mitochondrial disease, a rare genetic disorder affecting approximately one in 5,000 people, at the age of 14.
